NDC properties for "dorzolamide 2 % / timolol 0.5 % Ophthalmic Solution" (RxCUI 1923432)
About this data
The tables show NDC propoerties for dorzolamide 2 % / timolol 0.5 % Ophthalmic Solution with the RxCUI 1923432
This product uses publicly available data from the U.S. National Library of Medicine (NLM), National Institutes of Health, Department of Health and Human Services; NLM is not responsible for the product and does not endorse or recommend this or any other product
Details for dorzolamide 2 % / timolol 0.5 % Ophthalmic Solution (RxCUI 1923432)
ANDA | ANDA077847 |
---|---|
ANDA | ANDA090037 |
ANDA | ANDA090604 |
ANDA | ANDA202054 |
ANDA | ANDA204777 |
ANDA | ANDA205295 |
ANDA | ANDA207523 |
ANDA | ANDA207629 |
ANDA | ANDA213099 |
ANDA | ANDA215520 |
MMSL_CODE | BD6611 |
MMSL_CODE | CD6611 |
RxCUI | 1923432 |
SNOMEDCT | 330734009 |
SPL_SET_ID | 02d89d37-cbca-4e06-83ef-2a10f988f1ea |
SPL_SET_ID | 09dbed18-9076-4891-93a7-d14bb2217926 |
SPL_SET_ID | 0b75a79a-e048-4bf1-b02b-a72a8b8a0b3b |
SPL_SET_ID | 17f04726-725f-4839-911d-47fc5e02baae |
SPL_SET_ID | 2a236f05-1ee1-4180-9d80-31518d2204c7 |
SPL_SET_ID | 2b1fa44a-3890-4634-bcfc-c7310b51128e |
SPL_SET_ID | 2d5dcaa5-97ee-40c3-aa29-fcfb91fb78e1 |
SPL_SET_ID | 3206f5f4-103f-4f04-9c95-35cf17e7a3eb |
SPL_SET_ID | 6b20c356-5f80-4cb9-87d0-02abd24b623c |
SPL_SET_ID | 6b9c446e-7068-479b-8611-aead7a8d2f50 |
SPL_SET_ID | 78f39126-3e3b-4633-a4e0-c1f09a794eec |
SPL_SET_ID | 7f6ab3f6-3644-434c-b6cf-e4f111d18962 |
SPL_SET_ID | 8cdf22c8-75ca-404e-b354-9e254690d0e7 |
SPL_SET_ID | a5c104e7-4d99-49ec-80bf-eccea69b4c79 |
SPL_SET_ID | adf59642-b978-4bce-bdf2-7ee1d12c45a3 |
SPL_SET_ID | be8b1a47-3342-4072-b67c-6d1374d5d4d6 |
SPL_SET_ID | c9ae08c5-275d-44b3-9d1e-5d8fedc21b96 |
SPL_SET_ID | cf0c5cb6-7e40-454b-9f2a-a05832bfa5db |
SPL_SET_ID | efab039e-a69d-4306-8305-b1d27781cfe0 |
SPL_SET_ID | f45cce05-fb47-4607-b68e-5a3d47e7235a |
SPL_SET_ID | ff76c0cf-256c-4015-94f4-405f0c46205f |
VUID | 4013217 |
VUID | 4029171 |
Prescribable Synonym | dorzolamide HCl 2 % / timolol maleate 0.5 % Ophthalmic Solution |
RXNAV_STR | dorzolamide 20 MG/ML / timolol 5 MG/ML Ophthalmic Solution |
RxNorm Name | dorzolamide 20 MG/ML / timolol 5 MG/ML Ophthalmic Solution |
RxNorm Synonym | dorzolamide 2 % / timolol 0.5 % Ophthalmic Solution |
RxNorm Synonym | dorzolamide 20 MG/ML (as dorzolamide HCl 22.26 MG/ML) / timolol 5 MG/ML (as timolol maleate 6.83 MG/ML) Ophthalmic Solution |
Related queries | Interactions (for RxCUI 1923432) |
NDC Properties
NDC Item 00527176373
NDC 9 | 0527-1763 |
---|---|
NDC 10 | 0527-1763-73 |
NDC Item | 00527176373 |
Packaging | 1 BOTTLE, DROPPER in 1 CARTON (0527-1763-73) / 10 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA201998 |
FDA SPL set id | 447745 |
Labeler | Lannett Company, Inc. |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2014-12-17 |
Marketing status | COMPLETED |
Related queries | Properties for NDC 9 0527-1763 |
NDC Item 00781605470
NDC 9 | 0781-6054 |
---|---|
NDC 10 | 0781-6054-70 |
NDC Item | 00781605470 |
Packaging | 1 BOTTLE, DROPPER in 1 CARTON (0781-6054-70) / 10 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA077847 |
Labeler | Sandoz Inc |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing status | COMPLETED |
Related queries | Properties for NDC 9 0781-6054 |
NDC Item 14445040510
NDC 9 | 14445-405 |
---|---|
NDC 10 | 14445-405-10 |
NDC Item | 14445040510 |
Packaging | 1 BOTTLE, DISPENSING in 1 CARTON (14445-405-10) / 10 mL in 1 BOTTLE, DISPENSING |
ANDA | ANDA202054 |
FDA SPL set id | 837670 |
Labeler | Indoco Remedies Limited |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2021-05-14 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 14445-405 |
NDC Item 24208048605
NDC 9 | 24208-486 |
---|---|
NDC 10 | 24208-486-05 |
NDC Item | 24208048605 |
Packaging | 1 BOTTLE, DROPPER in 1 CARTON (24208-486-05) / 5 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA090037 |
FDA SPL set id | 744119 |
Labeler | Bausch & Lomb Incorporated |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2009-07-14 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 24208-486 |
NDC Item 24208048610
NDC 9 | 24208-486 |
---|---|
NDC 10 | 24208-486-10 |
NDC Item | 24208048610 |
Packaging | 1 BOTTLE, DROPPER in 1 CARTON (24208-486-10) / 10 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA090037 |
FDA SPL set id | 744119 |
Labeler | Bausch & Lomb Incorporated |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2009-07-14 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 24208-486 |
NDC Item 42571014726
NDC 9 | 42571-147 |
---|---|
NDC 10 | 42571-147-26 |
NDC Item | 42571014726 |
Packaging | 1 BOTTLE in 1 CARTON (42571-147-26) / 10 mL in 1 BOTTLE |
ANDA | ANDA204777 |
COLORTEXT | white(colorless to nearly colorless) |
Color | C48325 __ |
FDA SPL set id | 812624 |
Labeler | Micro Labs Limited |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2020-06-15 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 42571-147 |
NDC Item 46708055310
NDC 9 | 46708-553 |
---|---|
NDC 10 | 46708-553-10 |
NDC Item | 46708055310 |
Packaging | 1 BOTTLE in 1 CARTON (46708-553-10) / 10 mL in 1 BOTTLE |
ANDA | ANDA213099 |
FDA SPL set id | 827356 |
Labeler | Alembic Pharmaceuticals Limited |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2021-05-04 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 46708-553 |
NDC Item 50090286700
NDC 9 | 50090-2867 |
---|---|
NDC 10 | 50090-2867-0 |
NDC Item | 50090286700 |
Packaging | 1 BOTTLE, DISPENSING in 1 CARTON (50090-2867-0) / 10 mL in 1 BOTTLE, DISPENSING |
ANDA | ANDA202054 |
FDA SPL set id | 302402 |
Labeler | A-S Medication Solutions LLC |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2015-02-17 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 50090-2867 |
NDC Item 50090637100
NDC 9 | 50090-6371 |
---|---|
NDC 10 | 50090-6371-0 |
NDC Item | 50090637100 |
Packaging | 1 BOTTLE, DROPPER in 1 CARTON (50090-6371-0) / 10 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA090037 |
FDA SPL set id | 826332 |
Labeler | A-S Medication Solutions |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2009-07-14 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 50090-6371 |
NDC Item 50090681400
NDC 9 | 50090-6814 |
---|---|
NDC 10 | 50090-6814-0 |
NDC Item | 50090681400 |
Packaging | 1 BOTTLE in 1 CARTON (50090-6814-0) / 10 mL in 1 BOTTLE |
ANDA | ANDA204777 |
COLORTEXT | white(colorless to nearly colorless) |
Color | C48325 __ |
FDA SPL set id | 746492 |
Labeler | A-S Medication Solutions |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2020-06-15 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 50090-6814 |
NDC Item 50383023310
NDC 9 | 50383-233 |
---|---|
NDC 10 | 50383-233-10 |
NDC Item | 50383023310 |
Packaging | 1 BOTTLE, DROPPER in 1 BOX (50383-233-10) / 10 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA077847 |
FDA SPL set id | 640641 |
Labeler | Akorn Operating Company LLC (dba Akorn) |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2008-10-28 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 50383-233 |
NDC Item 60429011510
NDC 9 | 60429-115 |
---|---|
NDC 10 | 60429-115-10 |
NDC Item | 60429011510 |
Packaging | 1 BOTTLE, DROPPER in 1 BOX (60429-115-10) / 10 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA077847 |
FDA SPL set id | 767171 |
Labeler | Golden State Medical Supply, Inc. |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2008-10-28 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 60429-115 |
NDC Item 61314003001
NDC 9 | 61314-030 |
---|---|
NDC 10 | 61314-030-01 |
NDC Item | 61314003001 |
Packaging | 5 mL in 1 BOTTLE (61314-030-01) |
ANDA | ANDA090604 |
FDA SPL set id | 622450 |
Labeler | Sandoz Inc |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2010-01-02 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 61314-030 |
NDC Item 61314003002
NDC 9 | 61314-030 |
---|---|
NDC 10 | 61314-030-02 |
NDC Item | 61314003002 |
Packaging | 10 mL in 1 BOTTLE (61314-030-02) |
ANDA | ANDA090604 |
FDA SPL set id | 622450 |
Labeler | Sandoz Inc |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2010-01-02 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 61314-030 |
NDC Item 62332055310
NDC 9 | 62332-553 |
---|---|
NDC 10 | 62332-553-10 |
NDC Item | 62332055310 |
Packaging | 1 BOTTLE in 1 CARTON (62332-553-10) / 10 mL in 1 BOTTLE |
ANDA | ANDA213099 |
FDA SPL set id | 827411 |
Labeler | Alembic Pharmaceuticals Inc. |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2021-05-04 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 62332-553 |
NDC Item 65862094601
NDC 9 | 65862-946 |
---|---|
NDC 10 | 65862-946-01 |
NDC Item | 65862094601 |
Packaging | 1 BOTTLE, DROPPER in 1 CARTON (65862-946-01) / 10 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA207629 |
FDA SPL set id | 788118 |
Labeler | Aurobindo Pharma Limited |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2021-05-14 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 65862-946 |
NDC Item 68083049001
NDC 9 | 68083-490 |
---|---|
NDC 10 | 68083-490-01 |
NDC Item | 68083049001 |
Packaging | 1 BOTTLE in 1 CARTON (68083-490-01) / 10 mL in 1 BOTTLE |
ANDA | ANDA215520 |
FDA SPL set id | 786662 |
Labeler | Gland Pharma Limited |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2022-09-19 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 68083-490 |
NDC Item 69315030505
NDC 9 | 69315-305 |
---|---|
NDC 10 | 69315-305-05 |
NDC Item | 69315030505 |
Packaging | 1 BOTTLE, PLASTIC in 1 CARTON (69315-305-05) / 5 mL in 1 BOTTLE, PLASTIC |
ANDA | ANDA205295 |
FDA SPL set id | 787995 |
Labeler | Leading Pharma, LLC |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2017-05-18 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 69315-305 |
NDC Item 69315030510
NDC 9 | 69315-305 |
---|---|
NDC 10 | 69315-305-10 |
NDC Item | 69315030510 |
Packaging | 1 BOTTLE, PLASTIC in 1 CARTON (69315-305-10) / 10 mL in 1 BOTTLE, PLASTIC |
ANDA | ANDA205295 |
FDA SPL set id | 787995 |
Labeler | Leading Pharma, LLC |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2017-05-18 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 69315-305 |
NDC Item 70069005101
NDC 9 | 70069-051 |
---|---|
NDC 10 | 70069-051-01 |
NDC Item | 70069005101 |
Packaging | 1 BOTTLE in 1 CARTON (70069-051-01) / 10 mL in 1 BOTTLE |
ANDA | ANDA207523 |
COLORTEXT | WHITE(A clear, colorless to nearly colorless solution) |
Color | C48325 __ |
FDA SPL set id | 755334 |
Labeler | Somerset Therapeutics, LLC |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2019-06-25 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 70069-051 |
NDC Item 70377008211
NDC 9 | 70377-082 |
---|---|
NDC 10 | 70377-082-11 |
NDC Item | 70377008211 |
Packaging | 1 BOTTLE, DISPENSING in 1 CARTON (70377-082-11) / 10 mL in 1 BOTTLE, DISPENSING |
ANDA | ANDA202054 |
FDA SPL set id | 611443 |
Labeler | Biocon Pharma Inc. |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2022-01-08 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 70377-082 |
NDC Item 71921022610
NDC 9 | 71921-226 |
---|---|
NDC 10 | 71921-226-10 |
NDC Item | 71921022610 |
Packaging | 1 BOTTLE, DISPENSING in 1 CARTON (71921-226-10) / 10 mL in 1 BOTTLE, DISPENSING |
ANDA | ANDA202054 |
FDA SPL set id | 724181 |
Labeler | Florida Pharmaceutical Products, LLC |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2023-08-16 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 71921-226 |
NDC Item 72162216602
NDC 9 | 72162-2166 |
---|---|
NDC 10 | 72162-2166-2 |
NDC Item | 72162216602 |
Packaging | 1 BOTTLE, DROPPER in 1 CARTON (72162-2166-2) / 10 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA090037 |
FDA SPL set id | 752883 |
Labeler | Bryant Ranch Prepack |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2009-07-14 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 72162-2166 |
NDC Item 72162218402
NDC 9 | 72162-2184 |
---|---|
NDC 10 | 72162-2184-2 |
NDC Item | 72162218402 |
Packaging | 10 mL in 1 BOTTLE (72162-2184-2) |
ANDA | ANDA090604 |
FDA SPL set id | 753279 |
Labeler | Bryant Ranch Prepack |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2010-01-02 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 72162-2184 |
NDC Item 72162238102
NDC 9 | 72162-2381 |
---|---|
NDC 10 | 72162-2381-2 |
NDC Item | 72162238102 |
Packaging | 1 BOTTLE in 1 CARTON (72162-2381-2) / 10 mL in 1 BOTTLE |
ANDA | ANDA204777 |
COLORTEXT | white(colorless to nearly colorless) |
Color | C48325 __ |
FDA SPL set id | 815591 |
Labeler | Bryant Ranch Prepack |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2020-06-15 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 72162-2381 |
NDC Item 00527176373
NDC 9 | 0527-1763 |
---|---|
NDC 10 | 0527-1763-73 |
NDC Item | 00527176373 |
Packaging | 1 BOTTLE, DROPPER in 1 CARTON (0527-1763-73) / 10 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA201998 |
FDA SPL set id | 447745 |
Labeler | Lannett Company, Inc. |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2014-12-17 |
Marketing status | COMPLETED |
Related queries | Properties for NDC 9 0527-1763 |
NDC Item 00781605470
NDC 9 | 0781-6054 |
---|---|
NDC 10 | 0781-6054-70 |
NDC Item | 00781605470 |
Packaging | 1 BOTTLE, DROPPER in 1 CARTON (0781-6054-70) / 10 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA077847 |
Labeler | Sandoz Inc |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing status | COMPLETED |
Related queries | Properties for NDC 9 0781-6054 |
NDC Item 14445040510
NDC 9 | 14445-405 |
---|---|
NDC 10 | 14445-405-10 |
NDC Item | 14445040510 |
Packaging | 1 BOTTLE, DISPENSING in 1 CARTON (14445-405-10) / 10 mL in 1 BOTTLE, DISPENSING |
ANDA | ANDA202054 |
FDA SPL set id | 837670 |
Labeler | Indoco Remedies Limited |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2021-05-14 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 14445-405 |
NDC Item 24208048605
NDC 9 | 24208-486 |
---|---|
NDC 10 | 24208-486-05 |
NDC Item | 24208048605 |
Packaging | 1 BOTTLE, DROPPER in 1 CARTON (24208-486-05) / 5 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA090037 |
FDA SPL set id | 744119 |
Labeler | Bausch & Lomb Incorporated |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2009-07-14 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 24208-486 |
NDC Item 24208048610
NDC 9 | 24208-486 |
---|---|
NDC 10 | 24208-486-10 |
NDC Item | 24208048610 |
Packaging | 1 BOTTLE, DROPPER in 1 CARTON (24208-486-10) / 10 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA090037 |
FDA SPL set id | 744119 |
Labeler | Bausch & Lomb Incorporated |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2009-07-14 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 24208-486 |
NDC Item 42571014726
NDC 9 | 42571-147 |
---|---|
NDC 10 | 42571-147-26 |
NDC Item | 42571014726 |
Packaging | 1 BOTTLE in 1 CARTON (42571-147-26) / 10 mL in 1 BOTTLE |
ANDA | ANDA204777 |
COLORTEXT | white(colorless to nearly colorless) |
Color | C48325 __ |
FDA SPL set id | 812624 |
Labeler | Micro Labs Limited |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2020-06-15 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 42571-147 |
NDC Item 46708055310
NDC 9 | 46708-553 |
---|---|
NDC 10 | 46708-553-10 |
NDC Item | 46708055310 |
Packaging | 1 BOTTLE in 1 CARTON (46708-553-10) / 10 mL in 1 BOTTLE |
ANDA | ANDA213099 |
FDA SPL set id | 827356 |
Labeler | Alembic Pharmaceuticals Limited |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2021-05-04 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 46708-553 |
NDC Item 50090286700
NDC 9 | 50090-2867 |
---|---|
NDC 10 | 50090-2867-0 |
NDC Item | 50090286700 |
Packaging | 1 BOTTLE, DISPENSING in 1 CARTON (50090-2867-0) / 10 mL in 1 BOTTLE, DISPENSING |
ANDA | ANDA202054 |
FDA SPL set id | 302402 |
Labeler | A-S Medication Solutions LLC |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2015-02-17 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 50090-2867 |
NDC Item 50090637100
NDC 9 | 50090-6371 |
---|---|
NDC 10 | 50090-6371-0 |
NDC Item | 50090637100 |
Packaging | 1 BOTTLE, DROPPER in 1 CARTON (50090-6371-0) / 10 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA090037 |
FDA SPL set id | 826332 |
Labeler | A-S Medication Solutions |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2009-07-14 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 50090-6371 |
NDC Item 50090681400
NDC 9 | 50090-6814 |
---|---|
NDC 10 | 50090-6814-0 |
NDC Item | 50090681400 |
Packaging | 1 BOTTLE in 1 CARTON (50090-6814-0) / 10 mL in 1 BOTTLE |
ANDA | ANDA204777 |
COLORTEXT | white(colorless to nearly colorless) |
Color | C48325 __ |
FDA SPL set id | 746492 |
Labeler | A-S Medication Solutions |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2020-06-15 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 50090-6814 |
NDC Item 50383023310
NDC 9 | 50383-233 |
---|---|
NDC 10 | 50383-233-10 |
NDC Item | 50383023310 |
Packaging | 1 BOTTLE, DROPPER in 1 BOX (50383-233-10) / 10 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA077847 |
FDA SPL set id | 640641 |
Labeler | Akorn Operating Company LLC (dba Akorn) |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2008-10-28 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 50383-233 |
NDC Item 60429011510
NDC 9 | 60429-115 |
---|---|
NDC 10 | 60429-115-10 |
NDC Item | 60429011510 |
Packaging | 1 BOTTLE, DROPPER in 1 BOX (60429-115-10) / 10 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA077847 |
FDA SPL set id | 767171 |
Labeler | Golden State Medical Supply, Inc. |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2008-10-28 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 60429-115 |
NDC Item 61314003001
NDC 9 | 61314-030 |
---|---|
NDC 10 | 61314-030-01 |
NDC Item | 61314003001 |
Packaging | 5 mL in 1 BOTTLE (61314-030-01) |
ANDA | ANDA090604 |
FDA SPL set id | 622450 |
Labeler | Sandoz Inc |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2010-01-02 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 61314-030 |
NDC Item 61314003002
NDC 9 | 61314-030 |
---|---|
NDC 10 | 61314-030-02 |
NDC Item | 61314003002 |
Packaging | 10 mL in 1 BOTTLE (61314-030-02) |
ANDA | ANDA090604 |
FDA SPL set id | 622450 |
Labeler | Sandoz Inc |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2010-01-02 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 61314-030 |
NDC Item 62332055310
NDC 9 | 62332-553 |
---|---|
NDC 10 | 62332-553-10 |
NDC Item | 62332055310 |
Packaging | 1 BOTTLE in 1 CARTON (62332-553-10) / 10 mL in 1 BOTTLE |
ANDA | ANDA213099 |
FDA SPL set id | 827411 |
Labeler | Alembic Pharmaceuticals Inc. |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2021-05-04 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 62332-553 |
NDC Item 65862094601
NDC 9 | 65862-946 |
---|---|
NDC 10 | 65862-946-01 |
NDC Item | 65862094601 |
Packaging | 1 BOTTLE, DROPPER in 1 CARTON (65862-946-01) / 10 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA207629 |
FDA SPL set id | 788118 |
Labeler | Aurobindo Pharma Limited |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2021-05-14 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 65862-946 |
NDC Item 68083049001
NDC 9 | 68083-490 |
---|---|
NDC 10 | 68083-490-01 |
NDC Item | 68083049001 |
Packaging | 1 BOTTLE in 1 CARTON (68083-490-01) / 10 mL in 1 BOTTLE |
ANDA | ANDA215520 |
FDA SPL set id | 786662 |
Labeler | Gland Pharma Limited |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2022-09-19 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 68083-490 |
NDC Item 69315030505
NDC 9 | 69315-305 |
---|---|
NDC 10 | 69315-305-05 |
NDC Item | 69315030505 |
Packaging | 1 BOTTLE, PLASTIC in 1 CARTON (69315-305-05) / 5 mL in 1 BOTTLE, PLASTIC |
ANDA | ANDA205295 |
FDA SPL set id | 787995 |
Labeler | Leading Pharma, LLC |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2017-05-18 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 69315-305 |
NDC Item 69315030510
NDC 9 | 69315-305 |
---|---|
NDC 10 | 69315-305-10 |
NDC Item | 69315030510 |
Packaging | 1 BOTTLE, PLASTIC in 1 CARTON (69315-305-10) / 10 mL in 1 BOTTLE, PLASTIC |
ANDA | ANDA205295 |
FDA SPL set id | 787995 |
Labeler | Leading Pharma, LLC |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2017-05-18 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 69315-305 |
NDC Item 70069005101
NDC 9 | 70069-051 |
---|---|
NDC 10 | 70069-051-01 |
NDC Item | 70069005101 |
Packaging | 1 BOTTLE in 1 CARTON (70069-051-01) / 10 mL in 1 BOTTLE |
ANDA | ANDA207523 |
COLORTEXT | WHITE(A clear, colorless to nearly colorless solution) |
Color | C48325 __ |
FDA SPL set id | 755334 |
Labeler | Somerset Therapeutics, LLC |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2019-06-25 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 70069-051 |
NDC Item 70377008211
NDC 9 | 70377-082 |
---|---|
NDC 10 | 70377-082-11 |
NDC Item | 70377008211 |
Packaging | 1 BOTTLE, DISPENSING in 1 CARTON (70377-082-11) / 10 mL in 1 BOTTLE, DISPENSING |
ANDA | ANDA202054 |
FDA SPL set id | 611443 |
Labeler | Biocon Pharma Inc. |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2022-01-08 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 70377-082 |
NDC Item 71921022610
NDC 9 | 71921-226 |
---|---|
NDC 10 | 71921-226-10 |
NDC Item | 71921022610 |
Packaging | 1 BOTTLE, DISPENSING in 1 CARTON (71921-226-10) / 10 mL in 1 BOTTLE, DISPENSING |
ANDA | ANDA202054 |
FDA SPL set id | 724181 |
Labeler | Florida Pharmaceutical Products, LLC |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2023-08-16 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 71921-226 |
NDC Item 72162216602
NDC 9 | 72162-2166 |
---|---|
NDC 10 | 72162-2166-2 |
NDC Item | 72162216602 |
Packaging | 1 BOTTLE, DROPPER in 1 CARTON (72162-2166-2) / 10 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA090037 |
FDA SPL set id | 752883 |
Labeler | Bryant Ranch Prepack |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2009-07-14 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 72162-2166 |
NDC Item 72162218402
NDC 9 | 72162-2184 |
---|---|
NDC 10 | 72162-2184-2 |
NDC Item | 72162218402 |
Packaging | 10 mL in 1 BOTTLE (72162-2184-2) |
ANDA | ANDA090604 |
FDA SPL set id | 753279 |
Labeler | Bryant Ranch Prepack |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2010-01-02 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 72162-2184 |
NDC Item 72162238102
NDC 9 | 72162-2381 |
---|---|
NDC 10 | 72162-2381-2 |
NDC Item | 72162238102 |
Packaging | 1 BOTTLE in 1 CARTON (72162-2381-2) / 10 mL in 1 BOTTLE |
ANDA | ANDA204777 |
COLORTEXT | white(colorless to nearly colorless) |
Color | C48325 __ |
FDA SPL set id | 815591 |
Labeler | Bryant Ranch Prepack |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2020-06-15 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 72162-2381 |
NDC Item 00527176373
NDC 9 | 0527-1763 |
---|---|
NDC 10 | 0527-1763-73 |
NDC Item | 00527176373 |
Packaging | 1 BOTTLE, DROPPER in 1 CARTON (0527-1763-73) / 10 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA201998 |
FDA SPL set id | 447745 |
Labeler | Lannett Company, Inc. |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2014-12-17 |
Marketing status | COMPLETED |
Related queries | Properties for NDC 9 0527-1763 |
NDC Item 00781605470
NDC 9 | 0781-6054 |
---|---|
NDC 10 | 0781-6054-70 |
NDC Item | 00781605470 |
Packaging | 1 BOTTLE, DROPPER in 1 CARTON (0781-6054-70) / 10 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA077847 |
Labeler | Sandoz Inc |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing status | COMPLETED |
Related queries | Properties for NDC 9 0781-6054 |
NDC Item 14445040510
NDC 9 | 14445-405 |
---|---|
NDC 10 | 14445-405-10 |
NDC Item | 14445040510 |
Packaging | 1 BOTTLE, DISPENSING in 1 CARTON (14445-405-10) / 10 mL in 1 BOTTLE, DISPENSING |
ANDA | ANDA202054 |
FDA SPL set id | 837670 |
Labeler | Indoco Remedies Limited |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2021-05-14 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 14445-405 |
NDC Item 24208048605
NDC 9 | 24208-486 |
---|---|
NDC 10 | 24208-486-05 |
NDC Item | 24208048605 |
Packaging | 1 BOTTLE, DROPPER in 1 CARTON (24208-486-05) / 5 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA090037 |
FDA SPL set id | 744119 |
Labeler | Bausch & Lomb Incorporated |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2009-07-14 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 24208-486 |
NDC Item 24208048610
NDC 9 | 24208-486 |
---|---|
NDC 10 | 24208-486-10 |
NDC Item | 24208048610 |
Packaging | 1 BOTTLE, DROPPER in 1 CARTON (24208-486-10) / 10 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA090037 |
FDA SPL set id | 744119 |
Labeler | Bausch & Lomb Incorporated |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2009-07-14 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 24208-486 |
NDC Item 42571014726
NDC 9 | 42571-147 |
---|---|
NDC 10 | 42571-147-26 |
NDC Item | 42571014726 |
Packaging | 1 BOTTLE in 1 CARTON (42571-147-26) / 10 mL in 1 BOTTLE |
ANDA | ANDA204777 |
COLORTEXT | white(colorless to nearly colorless) |
Color | C48325 __ |
FDA SPL set id | 812624 |
Labeler | Micro Labs Limited |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2020-06-15 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 42571-147 |
NDC Item 46708055310
NDC 9 | 46708-553 |
---|---|
NDC 10 | 46708-553-10 |
NDC Item | 46708055310 |
Packaging | 1 BOTTLE in 1 CARTON (46708-553-10) / 10 mL in 1 BOTTLE |
ANDA | ANDA213099 |
FDA SPL set id | 827356 |
Labeler | Alembic Pharmaceuticals Limited |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2021-05-04 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 46708-553 |
NDC Item 50090286700
NDC 9 | 50090-2867 |
---|---|
NDC 10 | 50090-2867-0 |
NDC Item | 50090286700 |
Packaging | 1 BOTTLE, DISPENSING in 1 CARTON (50090-2867-0) / 10 mL in 1 BOTTLE, DISPENSING |
ANDA | ANDA202054 |
FDA SPL set id | 302402 |
Labeler | A-S Medication Solutions LLC |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2015-02-17 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 50090-2867 |
NDC Item 50090637100
NDC 9 | 50090-6371 |
---|---|
NDC 10 | 50090-6371-0 |
NDC Item | 50090637100 |
Packaging | 1 BOTTLE, DROPPER in 1 CARTON (50090-6371-0) / 10 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA090037 |
FDA SPL set id | 826332 |
Labeler | A-S Medication Solutions |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2009-07-14 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 50090-6371 |
NDC Item 50090681400
NDC 9 | 50090-6814 |
---|---|
NDC 10 | 50090-6814-0 |
NDC Item | 50090681400 |
Packaging | 1 BOTTLE in 1 CARTON (50090-6814-0) / 10 mL in 1 BOTTLE |
ANDA | ANDA204777 |
COLORTEXT | white(colorless to nearly colorless) |
Color | C48325 __ |
FDA SPL set id | 746492 |
Labeler | A-S Medication Solutions |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2020-06-15 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 50090-6814 |
NDC Item 50383023310
NDC 9 | 50383-233 |
---|---|
NDC 10 | 50383-233-10 |
NDC Item | 50383023310 |
Packaging | 1 BOTTLE, DROPPER in 1 BOX (50383-233-10) / 10 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA077847 |
FDA SPL set id | 640641 |
Labeler | Akorn Operating Company LLC (dba Akorn) |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2008-10-28 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 50383-233 |
NDC Item 60429011510
NDC 9 | 60429-115 |
---|---|
NDC 10 | 60429-115-10 |
NDC Item | 60429011510 |
Packaging | 1 BOTTLE, DROPPER in 1 BOX (60429-115-10) / 10 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA077847 |
FDA SPL set id | 767171 |
Labeler | Golden State Medical Supply, Inc. |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2008-10-28 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 60429-115 |
NDC Item 61314003001
NDC 9 | 61314-030 |
---|---|
NDC 10 | 61314-030-01 |
NDC Item | 61314003001 |
Packaging | 5 mL in 1 BOTTLE (61314-030-01) |
ANDA | ANDA090604 |
FDA SPL set id | 622450 |
Labeler | Sandoz Inc |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2010-01-02 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 61314-030 |
NDC Item 61314003002
NDC 9 | 61314-030 |
---|---|
NDC 10 | 61314-030-02 |
NDC Item | 61314003002 |
Packaging | 10 mL in 1 BOTTLE (61314-030-02) |
ANDA | ANDA090604 |
FDA SPL set id | 622450 |
Labeler | Sandoz Inc |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2010-01-02 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 61314-030 |
NDC Item 62332055310
NDC 9 | 62332-553 |
---|---|
NDC 10 | 62332-553-10 |
NDC Item | 62332055310 |
Packaging | 1 BOTTLE in 1 CARTON (62332-553-10) / 10 mL in 1 BOTTLE |
ANDA | ANDA213099 |
FDA SPL set id | 827411 |
Labeler | Alembic Pharmaceuticals Inc. |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2021-05-04 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 62332-553 |
NDC Item 65862094601
NDC 9 | 65862-946 |
---|---|
NDC 10 | 65862-946-01 |
NDC Item | 65862094601 |
Packaging | 1 BOTTLE, DROPPER in 1 CARTON (65862-946-01) / 10 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA207629 |
FDA SPL set id | 788118 |
Labeler | Aurobindo Pharma Limited |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2021-05-14 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 65862-946 |
NDC Item 68083049001
NDC 9 | 68083-490 |
---|---|
NDC 10 | 68083-490-01 |
NDC Item | 68083049001 |
Packaging | 1 BOTTLE in 1 CARTON (68083-490-01) / 10 mL in 1 BOTTLE |
ANDA | ANDA215520 |
FDA SPL set id | 786662 |
Labeler | Gland Pharma Limited |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2022-09-19 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 68083-490 |
NDC Item 69315030505
NDC 9 | 69315-305 |
---|---|
NDC 10 | 69315-305-05 |
NDC Item | 69315030505 |
Packaging | 1 BOTTLE, PLASTIC in 1 CARTON (69315-305-05) / 5 mL in 1 BOTTLE, PLASTIC |
ANDA | ANDA205295 |
FDA SPL set id | 787995 |
Labeler | Leading Pharma, LLC |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2017-05-18 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 69315-305 |
NDC Item 69315030510
NDC 9 | 69315-305 |
---|---|
NDC 10 | 69315-305-10 |
NDC Item | 69315030510 |
Packaging | 1 BOTTLE, PLASTIC in 1 CARTON (69315-305-10) / 10 mL in 1 BOTTLE, PLASTIC |
ANDA | ANDA205295 |
FDA SPL set id | 787995 |
Labeler | Leading Pharma, LLC |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2017-05-18 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 69315-305 |
NDC Item 70069005101
NDC 9 | 70069-051 |
---|---|
NDC 10 | 70069-051-01 |
NDC Item | 70069005101 |
Packaging | 1 BOTTLE in 1 CARTON (70069-051-01) / 10 mL in 1 BOTTLE |
ANDA | ANDA207523 |
COLORTEXT | WHITE(A clear, colorless to nearly colorless solution) |
Color | C48325 __ |
FDA SPL set id | 755334 |
Labeler | Somerset Therapeutics, LLC |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2019-06-25 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 70069-051 |
NDC Item 70377008211
NDC 9 | 70377-082 |
---|---|
NDC 10 | 70377-082-11 |
NDC Item | 70377008211 |
Packaging | 1 BOTTLE, DISPENSING in 1 CARTON (70377-082-11) / 10 mL in 1 BOTTLE, DISPENSING |
ANDA | ANDA202054 |
FDA SPL set id | 611443 |
Labeler | Biocon Pharma Inc. |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2022-01-08 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 70377-082 |
NDC Item 71921022610
NDC 9 | 71921-226 |
---|---|
NDC 10 | 71921-226-10 |
NDC Item | 71921022610 |
Packaging | 1 BOTTLE, DISPENSING in 1 CARTON (71921-226-10) / 10 mL in 1 BOTTLE, DISPENSING |
ANDA | ANDA202054 |
FDA SPL set id | 724181 |
Labeler | Florida Pharmaceutical Products, LLC |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2023-08-16 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 71921-226 |
NDC Item 72162216602
NDC 9 | 72162-2166 |
---|---|
NDC 10 | 72162-2166-2 |
NDC Item | 72162216602 |
Packaging | 1 BOTTLE, DROPPER in 1 CARTON (72162-2166-2) / 10 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA090037 |
FDA SPL set id | 752883 |
Labeler | Bryant Ranch Prepack |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2009-07-14 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 72162-2166 |
NDC Item 72162218402
NDC 9 | 72162-2184 |
---|---|
NDC 10 | 72162-2184-2 |
NDC Item | 72162218402 |
Packaging | 10 mL in 1 BOTTLE (72162-2184-2) |
ANDA | ANDA090604 |
FDA SPL set id | 753279 |
Labeler | Bryant Ranch Prepack |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2010-01-02 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 72162-2184 |
NDC Item 72162238102
NDC 9 | 72162-2381 |
---|---|
NDC 10 | 72162-2381-2 |
NDC Item | 72162238102 |
Packaging | 1 BOTTLE in 1 CARTON (72162-2381-2) / 10 mL in 1 BOTTLE |
ANDA | ANDA204777 |
COLORTEXT | white(colorless to nearly colorless) |
Color | C48325 __ |
FDA SPL set id | 815591 |
Labeler | Bryant Ranch Prepack |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2020-06-15 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 72162-2381 |
NDC Item 00527176373
NDC 9 | 0527-1763 |
---|---|
NDC 10 | 0527-1763-73 |
NDC Item | 00527176373 |
Packaging | 1 BOTTLE, DROPPER in 1 CARTON (0527-1763-73) / 10 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA201998 |
FDA SPL set id | 447745 |
Labeler | Lannett Company, Inc. |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2014-12-17 |
Marketing status | COMPLETED |
Related queries | Properties for NDC 9 0527-1763 |
NDC Item 00781605470
NDC 9 | 0781-6054 |
---|---|
NDC 10 | 0781-6054-70 |
NDC Item | 00781605470 |
Packaging | 1 BOTTLE, DROPPER in 1 CARTON (0781-6054-70) / 10 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA077847 |
Labeler | Sandoz Inc |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing status | COMPLETED |
Related queries | Properties for NDC 9 0781-6054 |
NDC Item 14445040510
NDC 9 | 14445-405 |
---|---|
NDC 10 | 14445-405-10 |
NDC Item | 14445040510 |
Packaging | 1 BOTTLE, DISPENSING in 1 CARTON (14445-405-10) / 10 mL in 1 BOTTLE, DISPENSING |
ANDA | ANDA202054 |
FDA SPL set id | 837670 |
Labeler | Indoco Remedies Limited |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2021-05-14 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 14445-405 |
NDC Item 24208048605
NDC 9 | 24208-486 |
---|---|
NDC 10 | 24208-486-05 |
NDC Item | 24208048605 |
Packaging | 1 BOTTLE, DROPPER in 1 CARTON (24208-486-05) / 5 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA090037 |
FDA SPL set id | 744119 |
Labeler | Bausch & Lomb Incorporated |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2009-07-14 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 24208-486 |
NDC Item 24208048610
NDC 9 | 24208-486 |
---|---|
NDC 10 | 24208-486-10 |
NDC Item | 24208048610 |
Packaging | 1 BOTTLE, DROPPER in 1 CARTON (24208-486-10) / 10 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA090037 |
FDA SPL set id | 744119 |
Labeler | Bausch & Lomb Incorporated |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2009-07-14 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 24208-486 |
NDC Item 42571014726
NDC 9 | 42571-147 |
---|---|
NDC 10 | 42571-147-26 |
NDC Item | 42571014726 |
Packaging | 1 BOTTLE in 1 CARTON (42571-147-26) / 10 mL in 1 BOTTLE |
ANDA | ANDA204777 |
COLORTEXT | white(colorless to nearly colorless) |
Color | C48325 __ |
FDA SPL set id | 812624 |
Labeler | Micro Labs Limited |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2020-06-15 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 42571-147 |
NDC Item 46708055310
NDC 9 | 46708-553 |
---|---|
NDC 10 | 46708-553-10 |
NDC Item | 46708055310 |
Packaging | 1 BOTTLE in 1 CARTON (46708-553-10) / 10 mL in 1 BOTTLE |
ANDA | ANDA213099 |
FDA SPL set id | 827356 |
Labeler | Alembic Pharmaceuticals Limited |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2021-05-04 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 46708-553 |
NDC Item 50090286700
NDC 9 | 50090-2867 |
---|---|
NDC 10 | 50090-2867-0 |
NDC Item | 50090286700 |
Packaging | 1 BOTTLE, DISPENSING in 1 CARTON (50090-2867-0) / 10 mL in 1 BOTTLE, DISPENSING |
ANDA | ANDA202054 |
FDA SPL set id | 302402 |
Labeler | A-S Medication Solutions LLC |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2015-02-17 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 50090-2867 |
NDC Item 50090637100
NDC 9 | 50090-6371 |
---|---|
NDC 10 | 50090-6371-0 |
NDC Item | 50090637100 |
Packaging | 1 BOTTLE, DROPPER in 1 CARTON (50090-6371-0) / 10 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA090037 |
FDA SPL set id | 826332 |
Labeler | A-S Medication Solutions |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2009-07-14 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 50090-6371 |
NDC Item 50090681400
NDC 9 | 50090-6814 |
---|---|
NDC 10 | 50090-6814-0 |
NDC Item | 50090681400 |
Packaging | 1 BOTTLE in 1 CARTON (50090-6814-0) / 10 mL in 1 BOTTLE |
ANDA | ANDA204777 |
COLORTEXT | white(colorless to nearly colorless) |
Color | C48325 __ |
FDA SPL set id | 746492 |
Labeler | A-S Medication Solutions |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2020-06-15 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 50090-6814 |
NDC Item 50383023310
NDC 9 | 50383-233 |
---|---|
NDC 10 | 50383-233-10 |
NDC Item | 50383023310 |
Packaging | 1 BOTTLE, DROPPER in 1 BOX (50383-233-10) / 10 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA077847 |
FDA SPL set id | 640641 |
Labeler | Akorn Operating Company LLC (dba Akorn) |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2008-10-28 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 50383-233 |
NDC Item 60429011510
NDC 9 | 60429-115 |
---|---|
NDC 10 | 60429-115-10 |
NDC Item | 60429011510 |
Packaging | 1 BOTTLE, DROPPER in 1 BOX (60429-115-10) / 10 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA077847 |
FDA SPL set id | 767171 |
Labeler | Golden State Medical Supply, Inc. |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2008-10-28 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 60429-115 |
NDC Item 61314003001
NDC 9 | 61314-030 |
---|---|
NDC 10 | 61314-030-01 |
NDC Item | 61314003001 |
Packaging | 5 mL in 1 BOTTLE (61314-030-01) |
ANDA | ANDA090604 |
FDA SPL set id | 622450 |
Labeler | Sandoz Inc |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2010-01-02 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 61314-030 |
NDC Item 61314003002
NDC 9 | 61314-030 |
---|---|
NDC 10 | 61314-030-02 |
NDC Item | 61314003002 |
Packaging | 10 mL in 1 BOTTLE (61314-030-02) |
ANDA | ANDA090604 |
FDA SPL set id | 622450 |
Labeler | Sandoz Inc |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2010-01-02 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 61314-030 |
NDC Item 62332055310
NDC 9 | 62332-553 |
---|---|
NDC 10 | 62332-553-10 |
NDC Item | 62332055310 |
Packaging | 1 BOTTLE in 1 CARTON (62332-553-10) / 10 mL in 1 BOTTLE |
ANDA | ANDA213099 |
FDA SPL set id | 827411 |
Labeler | Alembic Pharmaceuticals Inc. |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2021-05-04 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 62332-553 |
NDC Item 65862094601
NDC 9 | 65862-946 |
---|---|
NDC 10 | 65862-946-01 |
NDC Item | 65862094601 |
Packaging | 1 BOTTLE, DROPPER in 1 CARTON (65862-946-01) / 10 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA207629 |
FDA SPL set id | 788118 |
Labeler | Aurobindo Pharma Limited |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2021-05-14 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 65862-946 |
NDC Item 68083049001
NDC 9 | 68083-490 |
---|---|
NDC 10 | 68083-490-01 |
NDC Item | 68083049001 |
Packaging | 1 BOTTLE in 1 CARTON (68083-490-01) / 10 mL in 1 BOTTLE |
ANDA | ANDA215520 |
FDA SPL set id | 786662 |
Labeler | Gland Pharma Limited |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2022-09-19 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 68083-490 |
NDC Item 69315030505
NDC 9 | 69315-305 |
---|---|
NDC 10 | 69315-305-05 |
NDC Item | 69315030505 |
Packaging | 1 BOTTLE, PLASTIC in 1 CARTON (69315-305-05) / 5 mL in 1 BOTTLE, PLASTIC |
ANDA | ANDA205295 |
FDA SPL set id | 787995 |
Labeler | Leading Pharma, LLC |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2017-05-18 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 69315-305 |
NDC Item 69315030510
NDC 9 | 69315-305 |
---|---|
NDC 10 | 69315-305-10 |
NDC Item | 69315030510 |
Packaging | 1 BOTTLE, PLASTIC in 1 CARTON (69315-305-10) / 10 mL in 1 BOTTLE, PLASTIC |
ANDA | ANDA205295 |
FDA SPL set id | 787995 |
Labeler | Leading Pharma, LLC |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2017-05-18 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 69315-305 |
NDC Item 70069005101
NDC 9 | 70069-051 |
---|---|
NDC 10 | 70069-051-01 |
NDC Item | 70069005101 |
Packaging | 1 BOTTLE in 1 CARTON (70069-051-01) / 10 mL in 1 BOTTLE |
ANDA | ANDA207523 |
COLORTEXT | WHITE(A clear, colorless to nearly colorless solution) |
Color | C48325 __ |
FDA SPL set id | 755334 |
Labeler | Somerset Therapeutics, LLC |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2019-06-25 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 70069-051 |
NDC Item 70377008211
NDC 9 | 70377-082 |
---|---|
NDC 10 | 70377-082-11 |
NDC Item | 70377008211 |
Packaging | 1 BOTTLE, DISPENSING in 1 CARTON (70377-082-11) / 10 mL in 1 BOTTLE, DISPENSING |
ANDA | ANDA202054 |
FDA SPL set id | 611443 |
Labeler | Biocon Pharma Inc. |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2022-01-08 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 70377-082 |
NDC Item 71921022610
NDC 9 | 71921-226 |
---|---|
NDC 10 | 71921-226-10 |
NDC Item | 71921022610 |
Packaging | 1 BOTTLE, DISPENSING in 1 CARTON (71921-226-10) / 10 mL in 1 BOTTLE, DISPENSING |
ANDA | ANDA202054 |
FDA SPL set id | 724181 |
Labeler | Florida Pharmaceutical Products, LLC |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2023-08-16 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 71921-226 |
NDC Item 72162216602
NDC 9 | 72162-2166 |
---|---|
NDC 10 | 72162-2166-2 |
NDC Item | 72162216602 |
Packaging | 1 BOTTLE, DROPPER in 1 CARTON (72162-2166-2) / 10 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA090037 |
FDA SPL set id | 752883 |
Labeler | Bryant Ranch Prepack |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2009-07-14 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 72162-2166 |
NDC Item 72162218402
NDC 9 | 72162-2184 |
---|---|
NDC 10 | 72162-2184-2 |
NDC Item | 72162218402 |
Packaging | 10 mL in 1 BOTTLE (72162-2184-2) |
ANDA | ANDA090604 |
FDA SPL set id | 753279 |
Labeler | Bryant Ranch Prepack |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2010-01-02 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 72162-2184 |
NDC Item 72162238102
NDC 9 | 72162-2381 |
---|---|
NDC 10 | 72162-2381-2 |
NDC Item | 72162238102 |
Packaging | 1 BOTTLE in 1 CARTON (72162-2381-2) / 10 mL in 1 BOTTLE |
ANDA | ANDA204777 |
COLORTEXT | white(colorless to nearly colorless) |
Color | C48325 __ |
FDA SPL set id | 815591 |
Labeler | Bryant Ranch Prepack |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2020-06-15 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 72162-2381 |
NDC Item 00527176373
NDC 9 | 0527-1763 |
---|---|
NDC 10 | 0527-1763-73 |
NDC Item | 00527176373 |
Packaging | 1 BOTTLE, DROPPER in 1 CARTON (0527-1763-73) / 10 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA201998 |
FDA SPL set id | 447745 |
Labeler | Lannett Company, Inc. |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2014-12-17 |
Marketing status | COMPLETED |
Related queries | Properties for NDC 9 0527-1763 |
NDC Item 00781605470
NDC 9 | 0781-6054 |
---|---|
NDC 10 | 0781-6054-70 |
NDC Item | 00781605470 |
Packaging | 1 BOTTLE, DROPPER in 1 CARTON (0781-6054-70) / 10 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA077847 |
Labeler | Sandoz Inc |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing status | COMPLETED |
Related queries | Properties for NDC 9 0781-6054 |
NDC Item 14445040510
NDC 9 | 14445-405 |
---|---|
NDC 10 | 14445-405-10 |
NDC Item | 14445040510 |
Packaging | 1 BOTTLE, DISPENSING in 1 CARTON (14445-405-10) / 10 mL in 1 BOTTLE, DISPENSING |
ANDA | ANDA202054 |
FDA SPL set id | 837670 |
Labeler | Indoco Remedies Limited |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2021-05-14 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 14445-405 |
NDC Item 24208048605
NDC 9 | 24208-486 |
---|---|
NDC 10 | 24208-486-05 |
NDC Item | 24208048605 |
Packaging | 1 BOTTLE, DROPPER in 1 CARTON (24208-486-05) / 5 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA090037 |
FDA SPL set id | 744119 |
Labeler | Bausch & Lomb Incorporated |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2009-07-14 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 24208-486 |
NDC Item 24208048610
NDC 9 | 24208-486 |
---|---|
NDC 10 | 24208-486-10 |
NDC Item | 24208048610 |
Packaging | 1 BOTTLE, DROPPER in 1 CARTON (24208-486-10) / 10 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA090037 |
FDA SPL set id | 744119 |
Labeler | Bausch & Lomb Incorporated |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2009-07-14 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 24208-486 |
NDC Item 42571014726
NDC 9 | 42571-147 |
---|---|
NDC 10 | 42571-147-26 |
NDC Item | 42571014726 |
Packaging | 1 BOTTLE in 1 CARTON (42571-147-26) / 10 mL in 1 BOTTLE |
ANDA | ANDA204777 |
COLORTEXT | white(colorless to nearly colorless) |
Color | C48325 __ |
FDA SPL set id | 812624 |
Labeler | Micro Labs Limited |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2020-06-15 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 42571-147 |
NDC Item 46708055310
NDC 9 | 46708-553 |
---|---|
NDC 10 | 46708-553-10 |
NDC Item | 46708055310 |
Packaging | 1 BOTTLE in 1 CARTON (46708-553-10) / 10 mL in 1 BOTTLE |
ANDA | ANDA213099 |
FDA SPL set id | 827356 |
Labeler | Alembic Pharmaceuticals Limited |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2021-05-04 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 46708-553 |
NDC Item 50090286700
NDC 9 | 50090-2867 |
---|---|
NDC 10 | 50090-2867-0 |
NDC Item | 50090286700 |
Packaging | 1 BOTTLE, DISPENSING in 1 CARTON (50090-2867-0) / 10 mL in 1 BOTTLE, DISPENSING |
ANDA | ANDA202054 |
FDA SPL set id | 302402 |
Labeler | A-S Medication Solutions LLC |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2015-02-17 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 50090-2867 |
NDC Item 50090637100
NDC 9 | 50090-6371 |
---|---|
NDC 10 | 50090-6371-0 |
NDC Item | 50090637100 |
Packaging | 1 BOTTLE, DROPPER in 1 CARTON (50090-6371-0) / 10 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA090037 |
FDA SPL set id | 826332 |
Labeler | A-S Medication Solutions |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2009-07-14 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 50090-6371 |
NDC Item 50090681400
NDC 9 | 50090-6814 |
---|---|
NDC 10 | 50090-6814-0 |
NDC Item | 50090681400 |
Packaging | 1 BOTTLE in 1 CARTON (50090-6814-0) / 10 mL in 1 BOTTLE |
ANDA | ANDA204777 |
COLORTEXT | white(colorless to nearly colorless) |
Color | C48325 __ |
FDA SPL set id | 746492 |
Labeler | A-S Medication Solutions |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2020-06-15 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 50090-6814 |
NDC Item 50383023310
NDC 9 | 50383-233 |
---|---|
NDC 10 | 50383-233-10 |
NDC Item | 50383023310 |
Packaging | 1 BOTTLE, DROPPER in 1 BOX (50383-233-10) / 10 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA077847 |
FDA SPL set id | 640641 |
Labeler | Akorn Operating Company LLC (dba Akorn) |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2008-10-28 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 50383-233 |
NDC Item 60429011510
NDC 9 | 60429-115 |
---|---|
NDC 10 | 60429-115-10 |
NDC Item | 60429011510 |
Packaging | 1 BOTTLE, DROPPER in 1 BOX (60429-115-10) / 10 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA077847 |
FDA SPL set id | 767171 |
Labeler | Golden State Medical Supply, Inc. |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2008-10-28 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 60429-115 |
NDC Item 61314003001
NDC 9 | 61314-030 |
---|---|
NDC 10 | 61314-030-01 |
NDC Item | 61314003001 |
Packaging | 5 mL in 1 BOTTLE (61314-030-01) |
ANDA | ANDA090604 |
FDA SPL set id | 622450 |
Labeler | Sandoz Inc |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2010-01-02 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 61314-030 |
NDC Item 61314003002
NDC 9 | 61314-030 |
---|---|
NDC 10 | 61314-030-02 |
NDC Item | 61314003002 |
Packaging | 10 mL in 1 BOTTLE (61314-030-02) |
ANDA | ANDA090604 |
FDA SPL set id | 622450 |
Labeler | Sandoz Inc |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2010-01-02 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 61314-030 |
NDC Item 62332055310
NDC 9 | 62332-553 |
---|---|
NDC 10 | 62332-553-10 |
NDC Item | 62332055310 |
Packaging | 1 BOTTLE in 1 CARTON (62332-553-10) / 10 mL in 1 BOTTLE |
ANDA | ANDA213099 |
FDA SPL set id | 827411 |
Labeler | Alembic Pharmaceuticals Inc. |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2021-05-04 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 62332-553 |
NDC Item 65862094601
NDC 9 | 65862-946 |
---|---|
NDC 10 | 65862-946-01 |
NDC Item | 65862094601 |
Packaging | 1 BOTTLE, DROPPER in 1 CARTON (65862-946-01) / 10 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA207629 |
FDA SPL set id | 788118 |
Labeler | Aurobindo Pharma Limited |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2021-05-14 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 65862-946 |
NDC Item 68083049001
NDC 9 | 68083-490 |
---|---|
NDC 10 | 68083-490-01 |
NDC Item | 68083049001 |
Packaging | 1 BOTTLE in 1 CARTON (68083-490-01) / 10 mL in 1 BOTTLE |
ANDA | ANDA215520 |
FDA SPL set id | 786662 |
Labeler | Gland Pharma Limited |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2022-09-19 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 68083-490 |
NDC Item 69315030505
NDC 9 | 69315-305 |
---|---|
NDC 10 | 69315-305-05 |
NDC Item | 69315030505 |
Packaging | 1 BOTTLE, PLASTIC in 1 CARTON (69315-305-05) / 5 mL in 1 BOTTLE, PLASTIC |
ANDA | ANDA205295 |
FDA SPL set id | 787995 |
Labeler | Leading Pharma, LLC |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2017-05-18 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 69315-305 |
NDC Item 69315030510
NDC 9 | 69315-305 |
---|---|
NDC 10 | 69315-305-10 |
NDC Item | 69315030510 |
Packaging | 1 BOTTLE, PLASTIC in 1 CARTON (69315-305-10) / 10 mL in 1 BOTTLE, PLASTIC |
ANDA | ANDA205295 |
FDA SPL set id | 787995 |
Labeler | Leading Pharma, LLC |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2017-05-18 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 69315-305 |
NDC Item 70069005101
NDC 9 | 70069-051 |
---|---|
NDC 10 | 70069-051-01 |
NDC Item | 70069005101 |
Packaging | 1 BOTTLE in 1 CARTON (70069-051-01) / 10 mL in 1 BOTTLE |
ANDA | ANDA207523 |
COLORTEXT | WHITE(A clear, colorless to nearly colorless solution) |
Color | C48325 __ |
FDA SPL set id | 755334 |
Labeler | Somerset Therapeutics, LLC |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2019-06-25 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 70069-051 |
NDC Item 70377008211
NDC 9 | 70377-082 |
---|---|
NDC 10 | 70377-082-11 |
NDC Item | 70377008211 |
Packaging | 1 BOTTLE, DISPENSING in 1 CARTON (70377-082-11) / 10 mL in 1 BOTTLE, DISPENSING |
ANDA | ANDA202054 |
FDA SPL set id | 611443 |
Labeler | Biocon Pharma Inc. |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2022-01-08 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 70377-082 |
NDC Item 71921022610
NDC 9 | 71921-226 |
---|---|
NDC 10 | 71921-226-10 |
NDC Item | 71921022610 |
Packaging | 1 BOTTLE, DISPENSING in 1 CARTON (71921-226-10) / 10 mL in 1 BOTTLE, DISPENSING |
ANDA | ANDA202054 |
FDA SPL set id | 724181 |
Labeler | Florida Pharmaceutical Products, LLC |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2023-08-16 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 71921-226 |
NDC Item 72162216602
NDC 9 | 72162-2166 |
---|---|
NDC 10 | 72162-2166-2 |
NDC Item | 72162216602 |
Packaging | 1 BOTTLE, DROPPER in 1 CARTON (72162-2166-2) / 10 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA090037 |
FDA SPL set id | 752883 |
Labeler | Bryant Ranch Prepack |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2009-07-14 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 72162-2166 |
NDC Item 72162218402
NDC 9 | 72162-2184 |
---|---|
NDC 10 | 72162-2184-2 |
NDC Item | 72162218402 |
Packaging | 10 mL in 1 BOTTLE (72162-2184-2) |
ANDA | ANDA090604 |
FDA SPL set id | 753279 |
Labeler | Bryant Ranch Prepack |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2010-01-02 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 72162-2184 |
NDC Item 72162238102
NDC 9 | 72162-2381 |
---|---|
NDC 10 | 72162-2381-2 |
NDC Item | 72162238102 |
Packaging | 1 BOTTLE in 1 CARTON (72162-2381-2) / 10 mL in 1 BOTTLE |
ANDA | ANDA204777 |
COLORTEXT | white(colorless to nearly colorless) |
Color | C48325 __ |
FDA SPL set id | 815591 |
Labeler | Bryant Ranch Prepack |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2020-06-15 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 72162-2381 |
NDC Item 00527176373
NDC 9 | 0527-1763 |
---|---|
NDC 10 | 0527-1763-73 |
NDC Item | 00527176373 |
Packaging | 1 BOTTLE, DROPPER in 1 CARTON (0527-1763-73) / 10 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA201998 |
FDA SPL set id | 447745 |
Labeler | Lannett Company, Inc. |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2014-12-17 |
Marketing status | COMPLETED |
Related queries | Properties for NDC 9 0527-1763 |
NDC Item 00781605470
NDC 9 | 0781-6054 |
---|---|
NDC 10 | 0781-6054-70 |
NDC Item | 00781605470 |
Packaging | 1 BOTTLE, DROPPER in 1 CARTON (0781-6054-70) / 10 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA077847 |
Labeler | Sandoz Inc |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing status | COMPLETED |
Related queries | Properties for NDC 9 0781-6054 |
NDC Item 14445040510
NDC 9 | 14445-405 |
---|---|
NDC 10 | 14445-405-10 |
NDC Item | 14445040510 |
Packaging | 1 BOTTLE, DISPENSING in 1 CARTON (14445-405-10) / 10 mL in 1 BOTTLE, DISPENSING |
ANDA | ANDA202054 |
FDA SPL set id | 837670 |
Labeler | Indoco Remedies Limited |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2021-05-14 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 14445-405 |
NDC Item 24208048605
NDC 9 | 24208-486 |
---|---|
NDC 10 | 24208-486-05 |
NDC Item | 24208048605 |
Packaging | 1 BOTTLE, DROPPER in 1 CARTON (24208-486-05) / 5 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA090037 |
FDA SPL set id | 744119 |
Labeler | Bausch & Lomb Incorporated |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2009-07-14 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 24208-486 |
NDC Item 24208048610
NDC 9 | 24208-486 |
---|---|
NDC 10 | 24208-486-10 |
NDC Item | 24208048610 |
Packaging | 1 BOTTLE, DROPPER in 1 CARTON (24208-486-10) / 10 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA090037 |
FDA SPL set id | 744119 |
Labeler | Bausch & Lomb Incorporated |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2009-07-14 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 24208-486 |
NDC Item 42571014726
NDC 9 | 42571-147 |
---|---|
NDC 10 | 42571-147-26 |
NDC Item | 42571014726 |
Packaging | 1 BOTTLE in 1 CARTON (42571-147-26) / 10 mL in 1 BOTTLE |
ANDA | ANDA204777 |
COLORTEXT | white(colorless to nearly colorless) |
Color | C48325 __ |
FDA SPL set id | 812624 |
Labeler | Micro Labs Limited |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2020-06-15 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 42571-147 |
NDC Item 46708055310
NDC 9 | 46708-553 |
---|---|
NDC 10 | 46708-553-10 |
NDC Item | 46708055310 |
Packaging | 1 BOTTLE in 1 CARTON (46708-553-10) / 10 mL in 1 BOTTLE |
ANDA | ANDA213099 |
FDA SPL set id | 827356 |
Labeler | Alembic Pharmaceuticals Limited |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2021-05-04 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 46708-553 |
NDC Item 50090286700
NDC 9 | 50090-2867 |
---|---|
NDC 10 | 50090-2867-0 |
NDC Item | 50090286700 |
Packaging | 1 BOTTLE, DISPENSING in 1 CARTON (50090-2867-0) / 10 mL in 1 BOTTLE, DISPENSING |
ANDA | ANDA202054 |
FDA SPL set id | 302402 |
Labeler | A-S Medication Solutions LLC |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2015-02-17 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 50090-2867 |
NDC Item 50090637100
NDC 9 | 50090-6371 |
---|---|
NDC 10 | 50090-6371-0 |
NDC Item | 50090637100 |
Packaging | 1 BOTTLE, DROPPER in 1 CARTON (50090-6371-0) / 10 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA090037 |
FDA SPL set id | 826332 |
Labeler | A-S Medication Solutions |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2009-07-14 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 50090-6371 |
NDC Item 50090681400
NDC 9 | 50090-6814 |
---|---|
NDC 10 | 50090-6814-0 |
NDC Item | 50090681400 |
Packaging | 1 BOTTLE in 1 CARTON (50090-6814-0) / 10 mL in 1 BOTTLE |
ANDA | ANDA204777 |
COLORTEXT | white(colorless to nearly colorless) |
Color | C48325 __ |
FDA SPL set id | 746492 |
Labeler | A-S Medication Solutions |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2020-06-15 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 50090-6814 |
NDC Item 50383023310
NDC 9 | 50383-233 |
---|---|
NDC 10 | 50383-233-10 |
NDC Item | 50383023310 |
Packaging | 1 BOTTLE, DROPPER in 1 BOX (50383-233-10) / 10 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA077847 |
FDA SPL set id | 640641 |
Labeler | Akorn Operating Company LLC (dba Akorn) |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2008-10-28 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 50383-233 |
NDC Item 60429011510
NDC 9 | 60429-115 |
---|---|
NDC 10 | 60429-115-10 |
NDC Item | 60429011510 |
Packaging | 1 BOTTLE, DROPPER in 1 BOX (60429-115-10) / 10 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA077847 |
FDA SPL set id | 767171 |
Labeler | Golden State Medical Supply, Inc. |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2008-10-28 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 60429-115 |
NDC Item 61314003001
NDC 9 | 61314-030 |
---|---|
NDC 10 | 61314-030-01 |
NDC Item | 61314003001 |
Packaging | 5 mL in 1 BOTTLE (61314-030-01) |
ANDA | ANDA090604 |
FDA SPL set id | 622450 |
Labeler | Sandoz Inc |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2010-01-02 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 61314-030 |
NDC Item 61314003002
NDC 9 | 61314-030 |
---|---|
NDC 10 | 61314-030-02 |
NDC Item | 61314003002 |
Packaging | 10 mL in 1 BOTTLE (61314-030-02) |
ANDA | ANDA090604 |
FDA SPL set id | 622450 |
Labeler | Sandoz Inc |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2010-01-02 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 61314-030 |
NDC Item 62332055310
NDC 9 | 62332-553 |
---|---|
NDC 10 | 62332-553-10 |
NDC Item | 62332055310 |
Packaging | 1 BOTTLE in 1 CARTON (62332-553-10) / 10 mL in 1 BOTTLE |
ANDA | ANDA213099 |
FDA SPL set id | 827411 |
Labeler | Alembic Pharmaceuticals Inc. |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2021-05-04 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 62332-553 |
NDC Item 65862094601
NDC 9 | 65862-946 |
---|---|
NDC 10 | 65862-946-01 |
NDC Item | 65862094601 |
Packaging | 1 BOTTLE, DROPPER in 1 CARTON (65862-946-01) / 10 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA207629 |
FDA SPL set id | 788118 |
Labeler | Aurobindo Pharma Limited |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2021-05-14 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 65862-946 |
NDC Item 68083049001
NDC 9 | 68083-490 |
---|---|
NDC 10 | 68083-490-01 |
NDC Item | 68083049001 |
Packaging | 1 BOTTLE in 1 CARTON (68083-490-01) / 10 mL in 1 BOTTLE |
ANDA | ANDA215520 |
FDA SPL set id | 786662 |
Labeler | Gland Pharma Limited |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2022-09-19 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 68083-490 |
NDC Item 69315030505
NDC 9 | 69315-305 |
---|---|
NDC 10 | 69315-305-05 |
NDC Item | 69315030505 |
Packaging | 1 BOTTLE, PLASTIC in 1 CARTON (69315-305-05) / 5 mL in 1 BOTTLE, PLASTIC |
ANDA | ANDA205295 |
FDA SPL set id | 787995 |
Labeler | Leading Pharma, LLC |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2017-05-18 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 69315-305 |
NDC Item 69315030510
NDC 9 | 69315-305 |
---|---|
NDC 10 | 69315-305-10 |
NDC Item | 69315030510 |
Packaging | 1 BOTTLE, PLASTIC in 1 CARTON (69315-305-10) / 10 mL in 1 BOTTLE, PLASTIC |
ANDA | ANDA205295 |
FDA SPL set id | 787995 |
Labeler | Leading Pharma, LLC |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2017-05-18 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 69315-305 |
NDC Item 70069005101
NDC 9 | 70069-051 |
---|---|
NDC 10 | 70069-051-01 |
NDC Item | 70069005101 |
Packaging | 1 BOTTLE in 1 CARTON (70069-051-01) / 10 mL in 1 BOTTLE |
ANDA | ANDA207523 |
COLORTEXT | WHITE(A clear, colorless to nearly colorless solution) |
Color | C48325 __ |
FDA SPL set id | 755334 |
Labeler | Somerset Therapeutics, LLC |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2019-06-25 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 70069-051 |
NDC Item 70377008211
NDC 9 | 70377-082 |
---|---|
NDC 10 | 70377-082-11 |
NDC Item | 70377008211 |
Packaging | 1 BOTTLE, DISPENSING in 1 CARTON (70377-082-11) / 10 mL in 1 BOTTLE, DISPENSING |
ANDA | ANDA202054 |
FDA SPL set id | 611443 |
Labeler | Biocon Pharma Inc. |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2022-01-08 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 70377-082 |
NDC Item 71921022610
NDC 9 | 71921-226 |
---|---|
NDC 10 | 71921-226-10 |
NDC Item | 71921022610 |
Packaging | 1 BOTTLE, DISPENSING in 1 CARTON (71921-226-10) / 10 mL in 1 BOTTLE, DISPENSING |
ANDA | ANDA202054 |
FDA SPL set id | 724181 |
Labeler | Florida Pharmaceutical Products, LLC |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2023-08-16 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 71921-226 |
NDC Item 72162216602
NDC 9 | 72162-2166 |
---|---|
NDC 10 | 72162-2166-2 |
NDC Item | 72162216602 |
Packaging | 1 BOTTLE, DROPPER in 1 CARTON (72162-2166-2) / 10 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA090037 |
FDA SPL set id | 752883 |
Labeler | Bryant Ranch Prepack |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2009-07-14 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 72162-2166 |
NDC Item 72162218402
NDC 9 | 72162-2184 |
---|---|
NDC 10 | 72162-2184-2 |
NDC Item | 72162218402 |
Packaging | 10 mL in 1 BOTTLE (72162-2184-2) |
ANDA | ANDA090604 |
FDA SPL set id | 753279 |
Labeler | Bryant Ranch Prepack |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2010-01-02 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 72162-2184 |
NDC Item 72162238102
NDC 9 | 72162-2381 |
---|---|
NDC 10 | 72162-2381-2 |
NDC Item | 72162238102 |
Packaging | 1 BOTTLE in 1 CARTON (72162-2381-2) / 10 mL in 1 BOTTLE |
ANDA | ANDA204777 |
COLORTEXT | white(colorless to nearly colorless) |
Color | C48325 __ |
FDA SPL set id | 815591 |
Labeler | Bryant Ranch Prepack |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2020-06-15 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 72162-2381 |
NDC Item 00527176373
NDC 9 | 0527-1763 |
---|---|
NDC 10 | 0527-1763-73 |
NDC Item | 00527176373 |
Packaging | 1 BOTTLE, DROPPER in 1 CARTON (0527-1763-73) / 10 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA201998 |
FDA SPL set id | 447745 |
Labeler | Lannett Company, Inc. |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2014-12-17 |
Marketing status | COMPLETED |
Related queries | Properties for NDC 9 0527-1763 |
NDC Item 00781605470
NDC 9 | 0781-6054 |
---|---|
NDC 10 | 0781-6054-70 |
NDC Item | 00781605470 |
Packaging | 1 BOTTLE, DROPPER in 1 CARTON (0781-6054-70) / 10 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA077847 |
Labeler | Sandoz Inc |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing status | COMPLETED |
Related queries | Properties for NDC 9 0781-6054 |
NDC Item 14445040510
NDC 9 | 14445-405 |
---|---|
NDC 10 | 14445-405-10 |
NDC Item | 14445040510 |
Packaging | 1 BOTTLE, DISPENSING in 1 CARTON (14445-405-10) / 10 mL in 1 BOTTLE, DISPENSING |
ANDA | ANDA202054 |
FDA SPL set id | 837670 |
Labeler | Indoco Remedies Limited |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2021-05-14 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 14445-405 |
NDC Item 24208048605
NDC 9 | 24208-486 |
---|---|
NDC 10 | 24208-486-05 |
NDC Item | 24208048605 |
Packaging | 1 BOTTLE, DROPPER in 1 CARTON (24208-486-05) / 5 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA090037 |
FDA SPL set id | 744119 |
Labeler | Bausch & Lomb Incorporated |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2009-07-14 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 24208-486 |
NDC Item 24208048610
NDC 9 | 24208-486 |
---|---|
NDC 10 | 24208-486-10 |
NDC Item | 24208048610 |
Packaging | 1 BOTTLE, DROPPER in 1 CARTON (24208-486-10) / 10 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA090037 |
FDA SPL set id | 744119 |
Labeler | Bausch & Lomb Incorporated |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2009-07-14 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 24208-486 |
NDC Item 42571014726
NDC 9 | 42571-147 |
---|---|
NDC 10 | 42571-147-26 |
NDC Item | 42571014726 |
Packaging | 1 BOTTLE in 1 CARTON (42571-147-26) / 10 mL in 1 BOTTLE |
ANDA | ANDA204777 |
COLORTEXT | white(colorless to nearly colorless) |
Color | C48325 __ |
FDA SPL set id | 812624 |
Labeler | Micro Labs Limited |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2020-06-15 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 42571-147 |
NDC Item 46708055310
NDC 9 | 46708-553 |
---|---|
NDC 10 | 46708-553-10 |
NDC Item | 46708055310 |
Packaging | 1 BOTTLE in 1 CARTON (46708-553-10) / 10 mL in 1 BOTTLE |
ANDA | ANDA213099 |
FDA SPL set id | 827356 |
Labeler | Alembic Pharmaceuticals Limited |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2021-05-04 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 46708-553 |
NDC Item 50090286700
NDC 9 | 50090-2867 |
---|---|
NDC 10 | 50090-2867-0 |
NDC Item | 50090286700 |
Packaging | 1 BOTTLE, DISPENSING in 1 CARTON (50090-2867-0) / 10 mL in 1 BOTTLE, DISPENSING |
ANDA | ANDA202054 |
FDA SPL set id | 302402 |
Labeler | A-S Medication Solutions LLC |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2015-02-17 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 50090-2867 |
NDC Item 50090637100
NDC 9 | 50090-6371 |
---|---|
NDC 10 | 50090-6371-0 |
NDC Item | 50090637100 |
Packaging | 1 BOTTLE, DROPPER in 1 CARTON (50090-6371-0) / 10 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA090037 |
FDA SPL set id | 826332 |
Labeler | A-S Medication Solutions |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2009-07-14 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 50090-6371 |
NDC Item 50090681400
NDC 9 | 50090-6814 |
---|---|
NDC 10 | 50090-6814-0 |
NDC Item | 50090681400 |
Packaging | 1 BOTTLE in 1 CARTON (50090-6814-0) / 10 mL in 1 BOTTLE |
ANDA | ANDA204777 |
COLORTEXT | white(colorless to nearly colorless) |
Color | C48325 __ |
FDA SPL set id | 746492 |
Labeler | A-S Medication Solutions |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2020-06-15 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 50090-6814 |
NDC Item 50383023310
NDC 9 | 50383-233 |
---|---|
NDC 10 | 50383-233-10 |
NDC Item | 50383023310 |
Packaging | 1 BOTTLE, DROPPER in 1 BOX (50383-233-10) / 10 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA077847 |
FDA SPL set id | 640641 |
Labeler | Akorn Operating Company LLC (dba Akorn) |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2008-10-28 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 50383-233 |
NDC Item 60429011510
NDC 9 | 60429-115 |
---|---|
NDC 10 | 60429-115-10 |
NDC Item | 60429011510 |
Packaging | 1 BOTTLE, DROPPER in 1 BOX (60429-115-10) / 10 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA077847 |
FDA SPL set id | 767171 |
Labeler | Golden State Medical Supply, Inc. |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2008-10-28 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 60429-115 |
NDC Item 61314003001
NDC 9 | 61314-030 |
---|---|
NDC 10 | 61314-030-01 |
NDC Item | 61314003001 |
Packaging | 5 mL in 1 BOTTLE (61314-030-01) |
ANDA | ANDA090604 |
FDA SPL set id | 622450 |
Labeler | Sandoz Inc |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2010-01-02 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 61314-030 |
NDC Item 61314003002
NDC 9 | 61314-030 |
---|---|
NDC 10 | 61314-030-02 |
NDC Item | 61314003002 |
Packaging | 10 mL in 1 BOTTLE (61314-030-02) |
ANDA | ANDA090604 |
FDA SPL set id | 622450 |
Labeler | Sandoz Inc |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2010-01-02 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 61314-030 |
NDC Item 62332055310
NDC 9 | 62332-553 |
---|---|
NDC 10 | 62332-553-10 |
NDC Item | 62332055310 |
Packaging | 1 BOTTLE in 1 CARTON (62332-553-10) / 10 mL in 1 BOTTLE |
ANDA | ANDA213099 |
FDA SPL set id | 827411 |
Labeler | Alembic Pharmaceuticals Inc. |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2021-05-04 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 62332-553 |
NDC Item 65862094601
NDC 9 | 65862-946 |
---|---|
NDC 10 | 65862-946-01 |
NDC Item | 65862094601 |
Packaging | 1 BOTTLE, DROPPER in 1 CARTON (65862-946-01) / 10 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA207629 |
FDA SPL set id | 788118 |
Labeler | Aurobindo Pharma Limited |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2021-05-14 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 65862-946 |
NDC Item 68083049001
NDC 9 | 68083-490 |
---|---|
NDC 10 | 68083-490-01 |
NDC Item | 68083049001 |
Packaging | 1 BOTTLE in 1 CARTON (68083-490-01) / 10 mL in 1 BOTTLE |
ANDA | ANDA215520 |
FDA SPL set id | 786662 |
Labeler | Gland Pharma Limited |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2022-09-19 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 68083-490 |
NDC Item 69315030505
NDC 9 | 69315-305 |
---|---|
NDC 10 | 69315-305-05 |
NDC Item | 69315030505 |
Packaging | 1 BOTTLE, PLASTIC in 1 CARTON (69315-305-05) / 5 mL in 1 BOTTLE, PLASTIC |
ANDA | ANDA205295 |
FDA SPL set id | 787995 |
Labeler | Leading Pharma, LLC |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2017-05-18 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 69315-305 |
NDC Item 69315030510
NDC 9 | 69315-305 |
---|---|
NDC 10 | 69315-305-10 |
NDC Item | 69315030510 |
Packaging | 1 BOTTLE, PLASTIC in 1 CARTON (69315-305-10) / 10 mL in 1 BOTTLE, PLASTIC |
ANDA | ANDA205295 |
FDA SPL set id | 787995 |
Labeler | Leading Pharma, LLC |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2017-05-18 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 69315-305 |
NDC Item 70069005101
NDC 9 | 70069-051 |
---|---|
NDC 10 | 70069-051-01 |
NDC Item | 70069005101 |
Packaging | 1 BOTTLE in 1 CARTON (70069-051-01) / 10 mL in 1 BOTTLE |
ANDA | ANDA207523 |
COLORTEXT | WHITE(A clear, colorless to nearly colorless solution) |
Color | C48325 __ |
FDA SPL set id | 755334 |
Labeler | Somerset Therapeutics, LLC |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2019-06-25 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 70069-051 |
NDC Item 70377008211
NDC 9 | 70377-082 |
---|---|
NDC 10 | 70377-082-11 |
NDC Item | 70377008211 |
Packaging | 1 BOTTLE, DISPENSING in 1 CARTON (70377-082-11) / 10 mL in 1 BOTTLE, DISPENSING |
ANDA | ANDA202054 |
FDA SPL set id | 611443 |
Labeler | Biocon Pharma Inc. |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2022-01-08 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 70377-082 |
NDC Item 71921022610
NDC 9 | 71921-226 |
---|---|
NDC 10 | 71921-226-10 |
NDC Item | 71921022610 |
Packaging | 1 BOTTLE, DISPENSING in 1 CARTON (71921-226-10) / 10 mL in 1 BOTTLE, DISPENSING |
ANDA | ANDA202054 |
FDA SPL set id | 724181 |
Labeler | Florida Pharmaceutical Products, LLC |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2023-08-16 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 71921-226 |
NDC Item 72162216602
NDC 9 | 72162-2166 |
---|---|
NDC 10 | 72162-2166-2 |
NDC Item | 72162216602 |
Packaging | 1 BOTTLE, DROPPER in 1 CARTON (72162-2166-2) / 10 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA090037 |
FDA SPL set id | 752883 |
Labeler | Bryant Ranch Prepack |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2009-07-14 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 72162-2166 |
NDC Item 72162218402
NDC 9 | 72162-2184 |
---|---|
NDC 10 | 72162-2184-2 |
NDC Item | 72162218402 |
Packaging | 10 mL in 1 BOTTLE (72162-2184-2) |
ANDA | ANDA090604 |
FDA SPL set id | 753279 |
Labeler | Bryant Ranch Prepack |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2010-01-02 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 72162-2184 |
NDC Item 72162238102
NDC 9 | 72162-2381 |
---|---|
NDC 10 | 72162-2381-2 |
NDC Item | 72162238102 |
Packaging | 1 BOTTLE in 1 CARTON (72162-2381-2) / 10 mL in 1 BOTTLE |
ANDA | ANDA204777 |
COLORTEXT | white(colorless to nearly colorless) |
Color | C48325 __ |
FDA SPL set id | 815591 |
Labeler | Bryant Ranch Prepack |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2020-06-15 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 72162-2381 |
NDC Item 00527176373
NDC 9 | 0527-1763 |
---|---|
NDC 10 | 0527-1763-73 |
NDC Item | 00527176373 |
Packaging | 1 BOTTLE, DROPPER in 1 CARTON (0527-1763-73) / 10 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA201998 |
FDA SPL set id | 447745 |
Labeler | Lannett Company, Inc. |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2014-12-17 |
Marketing status | COMPLETED |
Related queries | Properties for NDC 9 0527-1763 |
NDC Item 00781605470
NDC 9 | 0781-6054 |
---|---|
NDC 10 | 0781-6054-70 |
NDC Item | 00781605470 |
Packaging | 1 BOTTLE, DROPPER in 1 CARTON (0781-6054-70) / 10 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA077847 |
Labeler | Sandoz Inc |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing status | COMPLETED |
Related queries | Properties for NDC 9 0781-6054 |
NDC Item 14445040510
NDC 9 | 14445-405 |
---|---|
NDC 10 | 14445-405-10 |
NDC Item | 14445040510 |
Packaging | 1 BOTTLE, DISPENSING in 1 CARTON (14445-405-10) / 10 mL in 1 BOTTLE, DISPENSING |
ANDA | ANDA202054 |
FDA SPL set id | 837670 |
Labeler | Indoco Remedies Limited |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2021-05-14 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 14445-405 |
NDC Item 24208048605
NDC 9 | 24208-486 |
---|---|
NDC 10 | 24208-486-05 |
NDC Item | 24208048605 |
Packaging | 1 BOTTLE, DROPPER in 1 CARTON (24208-486-05) / 5 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA090037 |
FDA SPL set id | 744119 |
Labeler | Bausch & Lomb Incorporated |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2009-07-14 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 24208-486 |
NDC Item 24208048610
NDC 9 | 24208-486 |
---|---|
NDC 10 | 24208-486-10 |
NDC Item | 24208048610 |
Packaging | 1 BOTTLE, DROPPER in 1 CARTON (24208-486-10) / 10 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA090037 |
FDA SPL set id | 744119 |
Labeler | Bausch & Lomb Incorporated |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2009-07-14 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 24208-486 |
NDC Item 42571014726
NDC 9 | 42571-147 |
---|---|
NDC 10 | 42571-147-26 |
NDC Item | 42571014726 |
Packaging | 1 BOTTLE in 1 CARTON (42571-147-26) / 10 mL in 1 BOTTLE |
ANDA | ANDA204777 |
COLORTEXT | white(colorless to nearly colorless) |
Color | C48325 __ |
FDA SPL set id | 812624 |
Labeler | Micro Labs Limited |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2020-06-15 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 42571-147 |
NDC Item 46708055310
NDC 9 | 46708-553 |
---|---|
NDC 10 | 46708-553-10 |
NDC Item | 46708055310 |
Packaging | 1 BOTTLE in 1 CARTON (46708-553-10) / 10 mL in 1 BOTTLE |
ANDA | ANDA213099 |
FDA SPL set id | 827356 |
Labeler | Alembic Pharmaceuticals Limited |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2021-05-04 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 46708-553 |
NDC Item 50090286700
NDC 9 | 50090-2867 |
---|---|
NDC 10 | 50090-2867-0 |
NDC Item | 50090286700 |
Packaging | 1 BOTTLE, DISPENSING in 1 CARTON (50090-2867-0) / 10 mL in 1 BOTTLE, DISPENSING |
ANDA | ANDA202054 |
FDA SPL set id | 302402 |
Labeler | A-S Medication Solutions LLC |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2015-02-17 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 50090-2867 |
NDC Item 50090637100
NDC 9 | 50090-6371 |
---|---|
NDC 10 | 50090-6371-0 |
NDC Item | 50090637100 |
Packaging | 1 BOTTLE, DROPPER in 1 CARTON (50090-6371-0) / 10 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA090037 |
FDA SPL set id | 826332 |
Labeler | A-S Medication Solutions |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2009-07-14 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 50090-6371 |
NDC Item 50090681400
NDC 9 | 50090-6814 |
---|---|
NDC 10 | 50090-6814-0 |
NDC Item | 50090681400 |
Packaging | 1 BOTTLE in 1 CARTON (50090-6814-0) / 10 mL in 1 BOTTLE |
ANDA | ANDA204777 |
COLORTEXT | white(colorless to nearly colorless) |
Color | C48325 __ |
FDA SPL set id | 746492 |
Labeler | A-S Medication Solutions |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2020-06-15 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 50090-6814 |
NDC Item 50383023310
NDC 9 | 50383-233 |
---|---|
NDC 10 | 50383-233-10 |
NDC Item | 50383023310 |
Packaging | 1 BOTTLE, DROPPER in 1 BOX (50383-233-10) / 10 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA077847 |
FDA SPL set id | 640641 |
Labeler | Akorn Operating Company LLC (dba Akorn) |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2008-10-28 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 50383-233 |
NDC Item 60429011510
NDC 9 | 60429-115 |
---|---|
NDC 10 | 60429-115-10 |
NDC Item | 60429011510 |
Packaging | 1 BOTTLE, DROPPER in 1 BOX (60429-115-10) / 10 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA077847 |
FDA SPL set id | 767171 |
Labeler | Golden State Medical Supply, Inc. |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2008-10-28 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 60429-115 |
NDC Item 61314003001
NDC 9 | 61314-030 |
---|---|
NDC 10 | 61314-030-01 |
NDC Item | 61314003001 |
Packaging | 5 mL in 1 BOTTLE (61314-030-01) |
ANDA | ANDA090604 |
FDA SPL set id | 622450 |
Labeler | Sandoz Inc |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2010-01-02 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 61314-030 |
NDC Item 61314003002
NDC 9 | 61314-030 |
---|---|
NDC 10 | 61314-030-02 |
NDC Item | 61314003002 |
Packaging | 10 mL in 1 BOTTLE (61314-030-02) |
ANDA | ANDA090604 |
FDA SPL set id | 622450 |
Labeler | Sandoz Inc |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2010-01-02 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 61314-030 |
NDC Item 62332055310
NDC 9 | 62332-553 |
---|---|
NDC 10 | 62332-553-10 |
NDC Item | 62332055310 |
Packaging | 1 BOTTLE in 1 CARTON (62332-553-10) / 10 mL in 1 BOTTLE |
ANDA | ANDA213099 |
FDA SPL set id | 827411 |
Labeler | Alembic Pharmaceuticals Inc. |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2021-05-04 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 62332-553 |
NDC Item 65862094601
NDC 9 | 65862-946 |
---|---|
NDC 10 | 65862-946-01 |
NDC Item | 65862094601 |
Packaging | 1 BOTTLE, DROPPER in 1 CARTON (65862-946-01) / 10 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA207629 |
FDA SPL set id | 788118 |
Labeler | Aurobindo Pharma Limited |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2021-05-14 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 65862-946 |
NDC Item 68083049001
NDC 9 | 68083-490 |
---|---|
NDC 10 | 68083-490-01 |
NDC Item | 68083049001 |
Packaging | 1 BOTTLE in 1 CARTON (68083-490-01) / 10 mL in 1 BOTTLE |
ANDA | ANDA215520 |
FDA SPL set id | 786662 |
Labeler | Gland Pharma Limited |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2022-09-19 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 68083-490 |
NDC Item 69315030505
NDC 9 | 69315-305 |
---|---|
NDC 10 | 69315-305-05 |
NDC Item | 69315030505 |
Packaging | 1 BOTTLE, PLASTIC in 1 CARTON (69315-305-05) / 5 mL in 1 BOTTLE, PLASTIC |
ANDA | ANDA205295 |
FDA SPL set id | 787995 |
Labeler | Leading Pharma, LLC |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2017-05-18 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 69315-305 |
NDC Item 69315030510
NDC 9 | 69315-305 |
---|---|
NDC 10 | 69315-305-10 |
NDC Item | 69315030510 |
Packaging | 1 BOTTLE, PLASTIC in 1 CARTON (69315-305-10) / 10 mL in 1 BOTTLE, PLASTIC |
ANDA | ANDA205295 |
FDA SPL set id | 787995 |
Labeler | Leading Pharma, LLC |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2017-05-18 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 69315-305 |
NDC Item 70069005101
NDC 9 | 70069-051 |
---|---|
NDC 10 | 70069-051-01 |
NDC Item | 70069005101 |
Packaging | 1 BOTTLE in 1 CARTON (70069-051-01) / 10 mL in 1 BOTTLE |
ANDA | ANDA207523 |
COLORTEXT | WHITE(A clear, colorless to nearly colorless solution) |
Color | C48325 __ |
FDA SPL set id | 755334 |
Labeler | Somerset Therapeutics, LLC |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2019-06-25 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 70069-051 |
NDC Item 70377008211
NDC 9 | 70377-082 |
---|---|
NDC 10 | 70377-082-11 |
NDC Item | 70377008211 |
Packaging | 1 BOTTLE, DISPENSING in 1 CARTON (70377-082-11) / 10 mL in 1 BOTTLE, DISPENSING |
ANDA | ANDA202054 |
FDA SPL set id | 611443 |
Labeler | Biocon Pharma Inc. |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2022-01-08 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 70377-082 |
NDC Item 71921022610
NDC 9 | 71921-226 |
---|---|
NDC 10 | 71921-226-10 |
NDC Item | 71921022610 |
Packaging | 1 BOTTLE, DISPENSING in 1 CARTON (71921-226-10) / 10 mL in 1 BOTTLE, DISPENSING |
ANDA | ANDA202054 |
FDA SPL set id | 724181 |
Labeler | Florida Pharmaceutical Products, LLC |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2023-08-16 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 71921-226 |
NDC Item 72162216602
NDC 9 | 72162-2166 |
---|---|
NDC 10 | 72162-2166-2 |
NDC Item | 72162216602 |
Packaging | 1 BOTTLE, DROPPER in 1 CARTON (72162-2166-2) / 10 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA090037 |
FDA SPL set id | 752883 |
Labeler | Bryant Ranch Prepack |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2009-07-14 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 72162-2166 |
NDC Item 72162218402
NDC 9 | 72162-2184 |
---|---|
NDC 10 | 72162-2184-2 |
NDC Item | 72162218402 |
Packaging | 10 mL in 1 BOTTLE (72162-2184-2) |
ANDA | ANDA090604 |
FDA SPL set id | 753279 |
Labeler | Bryant Ranch Prepack |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2010-01-02 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 72162-2184 |
NDC Item 72162238102
NDC 9 | 72162-2381 |
---|---|
NDC 10 | 72162-2381-2 |
NDC Item | 72162238102 |
Packaging | 1 BOTTLE in 1 CARTON (72162-2381-2) / 10 mL in 1 BOTTLE |
ANDA | ANDA204777 |
COLORTEXT | white(colorless to nearly colorless) |
Color | C48325 __ |
FDA SPL set id | 815591 |
Labeler | Bryant Ranch Prepack |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2020-06-15 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 72162-2381 |
NDC Item 00527176373
NDC 9 | 0527-1763 |
---|---|
NDC 10 | 0527-1763-73 |
NDC Item | 00527176373 |
Packaging | 1 BOTTLE, DROPPER in 1 CARTON (0527-1763-73) / 10 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA201998 |
FDA SPL set id | 447745 |
Labeler | Lannett Company, Inc. |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2014-12-17 |
Marketing status | COMPLETED |
Related queries | Properties for NDC 9 0527-1763 |
NDC Item 00781605470
NDC 9 | 0781-6054 |
---|---|
NDC 10 | 0781-6054-70 |
NDC Item | 00781605470 |
Packaging | 1 BOTTLE, DROPPER in 1 CARTON (0781-6054-70) / 10 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA077847 |
Labeler | Sandoz Inc |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing status | COMPLETED |
Related queries | Properties for NDC 9 0781-6054 |
NDC Item 14445040510
NDC 9 | 14445-405 |
---|---|
NDC 10 | 14445-405-10 |
NDC Item | 14445040510 |
Packaging | 1 BOTTLE, DISPENSING in 1 CARTON (14445-405-10) / 10 mL in 1 BOTTLE, DISPENSING |
ANDA | ANDA202054 |
FDA SPL set id | 837670 |
Labeler | Indoco Remedies Limited |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2021-05-14 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 14445-405 |
NDC Item 24208048605
NDC 9 | 24208-486 |
---|---|
NDC 10 | 24208-486-05 |
NDC Item | 24208048605 |
Packaging | 1 BOTTLE, DROPPER in 1 CARTON (24208-486-05) / 5 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA090037 |
FDA SPL set id | 744119 |
Labeler | Bausch & Lomb Incorporated |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2009-07-14 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 24208-486 |
NDC Item 24208048610
NDC 9 | 24208-486 |
---|---|
NDC 10 | 24208-486-10 |
NDC Item | 24208048610 |
Packaging | 1 BOTTLE, DROPPER in 1 CARTON (24208-486-10) / 10 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA090037 |
FDA SPL set id | 744119 |
Labeler | Bausch & Lomb Incorporated |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2009-07-14 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 24208-486 |
NDC Item 42571014726
NDC 9 | 42571-147 |
---|---|
NDC 10 | 42571-147-26 |
NDC Item | 42571014726 |
Packaging | 1 BOTTLE in 1 CARTON (42571-147-26) / 10 mL in 1 BOTTLE |
ANDA | ANDA204777 |
COLORTEXT | white(colorless to nearly colorless) |
Color | C48325 __ |
FDA SPL set id | 812624 |
Labeler | Micro Labs Limited |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2020-06-15 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 42571-147 |
NDC Item 46708055310
NDC 9 | 46708-553 |
---|---|
NDC 10 | 46708-553-10 |
NDC Item | 46708055310 |
Packaging | 1 BOTTLE in 1 CARTON (46708-553-10) / 10 mL in 1 BOTTLE |
ANDA | ANDA213099 |
FDA SPL set id | 827356 |
Labeler | Alembic Pharmaceuticals Limited |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2021-05-04 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 46708-553 |
NDC Item 50090286700
NDC 9 | 50090-2867 |
---|---|
NDC 10 | 50090-2867-0 |
NDC Item | 50090286700 |
Packaging | 1 BOTTLE, DISPENSING in 1 CARTON (50090-2867-0) / 10 mL in 1 BOTTLE, DISPENSING |
ANDA | ANDA202054 |
FDA SPL set id | 302402 |
Labeler | A-S Medication Solutions LLC |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2015-02-17 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 50090-2867 |
NDC Item 50090637100
NDC 9 | 50090-6371 |
---|---|
NDC 10 | 50090-6371-0 |
NDC Item | 50090637100 |
Packaging | 1 BOTTLE, DROPPER in 1 CARTON (50090-6371-0) / 10 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA090037 |
FDA SPL set id | 826332 |
Labeler | A-S Medication Solutions |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2009-07-14 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 50090-6371 |
NDC Item 50090681400
NDC 9 | 50090-6814 |
---|---|
NDC 10 | 50090-6814-0 |
NDC Item | 50090681400 |
Packaging | 1 BOTTLE in 1 CARTON (50090-6814-0) / 10 mL in 1 BOTTLE |
ANDA | ANDA204777 |
COLORTEXT | white(colorless to nearly colorless) |
Color | C48325 __ |
FDA SPL set id | 746492 |
Labeler | A-S Medication Solutions |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2020-06-15 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 50090-6814 |
NDC Item 50383023310
NDC 9 | 50383-233 |
---|---|
NDC 10 | 50383-233-10 |
NDC Item | 50383023310 |
Packaging | 1 BOTTLE, DROPPER in 1 BOX (50383-233-10) / 10 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA077847 |
FDA SPL set id | 640641 |
Labeler | Akorn Operating Company LLC (dba Akorn) |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2008-10-28 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 50383-233 |
NDC Item 60429011510
NDC 9 | 60429-115 |
---|---|
NDC 10 | 60429-115-10 |
NDC Item | 60429011510 |
Packaging | 1 BOTTLE, DROPPER in 1 BOX (60429-115-10) / 10 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA077847 |
FDA SPL set id | 767171 |
Labeler | Golden State Medical Supply, Inc. |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2008-10-28 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 60429-115 |
NDC Item 61314003001
NDC 9 | 61314-030 |
---|---|
NDC 10 | 61314-030-01 |
NDC Item | 61314003001 |
Packaging | 5 mL in 1 BOTTLE (61314-030-01) |
ANDA | ANDA090604 |
FDA SPL set id | 622450 |
Labeler | Sandoz Inc |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2010-01-02 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 61314-030 |
NDC Item 61314003002
NDC 9 | 61314-030 |
---|---|
NDC 10 | 61314-030-02 |
NDC Item | 61314003002 |
Packaging | 10 mL in 1 BOTTLE (61314-030-02) |
ANDA | ANDA090604 |
FDA SPL set id | 622450 |
Labeler | Sandoz Inc |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2010-01-02 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 61314-030 |
NDC Item 62332055310
NDC 9 | 62332-553 |
---|---|
NDC 10 | 62332-553-10 |
NDC Item | 62332055310 |
Packaging | 1 BOTTLE in 1 CARTON (62332-553-10) / 10 mL in 1 BOTTLE |
ANDA | ANDA213099 |
FDA SPL set id | 827411 |
Labeler | Alembic Pharmaceuticals Inc. |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2021-05-04 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 62332-553 |
NDC Item 65862094601
NDC 9 | 65862-946 |
---|---|
NDC 10 | 65862-946-01 |
NDC Item | 65862094601 |
Packaging | 1 BOTTLE, DROPPER in 1 CARTON (65862-946-01) / 10 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA207629 |
FDA SPL set id | 788118 |
Labeler | Aurobindo Pharma Limited |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2021-05-14 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 65862-946 |
NDC Item 68083049001
NDC 9 | 68083-490 |
---|---|
NDC 10 | 68083-490-01 |
NDC Item | 68083049001 |
Packaging | 1 BOTTLE in 1 CARTON (68083-490-01) / 10 mL in 1 BOTTLE |
ANDA | ANDA215520 |
FDA SPL set id | 786662 |
Labeler | Gland Pharma Limited |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2022-09-19 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 68083-490 |
NDC Item 69315030505
NDC 9 | 69315-305 |
---|---|
NDC 10 | 69315-305-05 |
NDC Item | 69315030505 |
Packaging | 1 BOTTLE, PLASTIC in 1 CARTON (69315-305-05) / 5 mL in 1 BOTTLE, PLASTIC |
ANDA | ANDA205295 |
FDA SPL set id | 787995 |
Labeler | Leading Pharma, LLC |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2017-05-18 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 69315-305 |
NDC Item 69315030510
NDC 9 | 69315-305 |
---|---|
NDC 10 | 69315-305-10 |
NDC Item | 69315030510 |
Packaging | 1 BOTTLE, PLASTIC in 1 CARTON (69315-305-10) / 10 mL in 1 BOTTLE, PLASTIC |
ANDA | ANDA205295 |
FDA SPL set id | 787995 |
Labeler | Leading Pharma, LLC |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2017-05-18 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 69315-305 |
NDC Item 70069005101
NDC 9 | 70069-051 |
---|---|
NDC 10 | 70069-051-01 |
NDC Item | 70069005101 |
Packaging | 1 BOTTLE in 1 CARTON (70069-051-01) / 10 mL in 1 BOTTLE |
ANDA | ANDA207523 |
COLORTEXT | WHITE(A clear, colorless to nearly colorless solution) |
Color | C48325 __ |
FDA SPL set id | 755334 |
Labeler | Somerset Therapeutics, LLC |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2019-06-25 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 70069-051 |
NDC Item 70377008211
NDC 9 | 70377-082 |
---|---|
NDC 10 | 70377-082-11 |
NDC Item | 70377008211 |
Packaging | 1 BOTTLE, DISPENSING in 1 CARTON (70377-082-11) / 10 mL in 1 BOTTLE, DISPENSING |
ANDA | ANDA202054 |
FDA SPL set id | 611443 |
Labeler | Biocon Pharma Inc. |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2022-01-08 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 70377-082 |
NDC Item 71921022610
NDC 9 | 71921-226 |
---|---|
NDC 10 | 71921-226-10 |
NDC Item | 71921022610 |
Packaging | 1 BOTTLE, DISPENSING in 1 CARTON (71921-226-10) / 10 mL in 1 BOTTLE, DISPENSING |
ANDA | ANDA202054 |
FDA SPL set id | 724181 |
Labeler | Florida Pharmaceutical Products, LLC |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2023-08-16 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 71921-226 |
NDC Item 72162216602
NDC 9 | 72162-2166 |
---|---|
NDC 10 | 72162-2166-2 |
NDC Item | 72162216602 |
Packaging | 1 BOTTLE, DROPPER in 1 CARTON (72162-2166-2) / 10 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA090037 |
FDA SPL set id | 752883 |
Labeler | Bryant Ranch Prepack |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2009-07-14 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 72162-2166 |
NDC Item 72162218402
NDC 9 | 72162-2184 |
---|---|
NDC 10 | 72162-2184-2 |
NDC Item | 72162218402 |
Packaging | 10 mL in 1 BOTTLE (72162-2184-2) |
ANDA | ANDA090604 |
FDA SPL set id | 753279 |
Labeler | Bryant Ranch Prepack |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2010-01-02 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 72162-2184 |
NDC Item 72162238102
NDC 9 | 72162-2381 |
---|---|
NDC 10 | 72162-2381-2 |
NDC Item | 72162238102 |
Packaging | 1 BOTTLE in 1 CARTON (72162-2381-2) / 10 mL in 1 BOTTLE |
ANDA | ANDA204777 |
COLORTEXT | white(colorless to nearly colorless) |
Color | C48325 __ |
FDA SPL set id | 815591 |
Labeler | Bryant Ranch Prepack |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2020-06-15 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 72162-2381 |
NDC Item 00527176373
NDC 9 | 0527-1763 |
---|---|
NDC 10 | 0527-1763-73 |
NDC Item | 00527176373 |
Packaging | 1 BOTTLE, DROPPER in 1 CARTON (0527-1763-73) / 10 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA201998 |
FDA SPL set id | 447745 |
Labeler | Lannett Company, Inc. |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2014-12-17 |
Marketing status | COMPLETED |
Related queries | Properties for NDC 9 0527-1763 |
NDC Item 00781605470
NDC 9 | 0781-6054 |
---|---|
NDC 10 | 0781-6054-70 |
NDC Item | 00781605470 |
Packaging | 1 BOTTLE, DROPPER in 1 CARTON (0781-6054-70) / 10 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA077847 |
Labeler | Sandoz Inc |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing status | COMPLETED |
Related queries | Properties for NDC 9 0781-6054 |
NDC Item 14445040510
NDC 9 | 14445-405 |
---|---|
NDC 10 | 14445-405-10 |
NDC Item | 14445040510 |
Packaging | 1 BOTTLE, DISPENSING in 1 CARTON (14445-405-10) / 10 mL in 1 BOTTLE, DISPENSING |
ANDA | ANDA202054 |
FDA SPL set id | 837670 |
Labeler | Indoco Remedies Limited |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2021-05-14 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 14445-405 |
NDC Item 24208048605
NDC 9 | 24208-486 |
---|---|
NDC 10 | 24208-486-05 |
NDC Item | 24208048605 |
Packaging | 1 BOTTLE, DROPPER in 1 CARTON (24208-486-05) / 5 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA090037 |
FDA SPL set id | 744119 |
Labeler | Bausch & Lomb Incorporated |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2009-07-14 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 24208-486 |
NDC Item 24208048610
NDC 9 | 24208-486 |
---|---|
NDC 10 | 24208-486-10 |
NDC Item | 24208048610 |
Packaging | 1 BOTTLE, DROPPER in 1 CARTON (24208-486-10) / 10 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA090037 |
FDA SPL set id | 744119 |
Labeler | Bausch & Lomb Incorporated |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2009-07-14 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 24208-486 |
NDC Item 42571014726
NDC 9 | 42571-147 |
---|---|
NDC 10 | 42571-147-26 |
NDC Item | 42571014726 |
Packaging | 1 BOTTLE in 1 CARTON (42571-147-26) / 10 mL in 1 BOTTLE |
ANDA | ANDA204777 |
COLORTEXT | white(colorless to nearly colorless) |
Color | C48325 __ |
FDA SPL set id | 812624 |
Labeler | Micro Labs Limited |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2020-06-15 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 42571-147 |
NDC Item 46708055310
NDC 9 | 46708-553 |
---|---|
NDC 10 | 46708-553-10 |
NDC Item | 46708055310 |
Packaging | 1 BOTTLE in 1 CARTON (46708-553-10) / 10 mL in 1 BOTTLE |
ANDA | ANDA213099 |
FDA SPL set id | 827356 |
Labeler | Alembic Pharmaceuticals Limited |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2021-05-04 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 46708-553 |
NDC Item 50090286700
NDC 9 | 50090-2867 |
---|---|
NDC 10 | 50090-2867-0 |
NDC Item | 50090286700 |
Packaging | 1 BOTTLE, DISPENSING in 1 CARTON (50090-2867-0) / 10 mL in 1 BOTTLE, DISPENSING |
ANDA | ANDA202054 |
FDA SPL set id | 302402 |
Labeler | A-S Medication Solutions LLC |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2015-02-17 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 50090-2867 |
NDC Item 50090637100
NDC 9 | 50090-6371 |
---|---|
NDC 10 | 50090-6371-0 |
NDC Item | 50090637100 |
Packaging | 1 BOTTLE, DROPPER in 1 CARTON (50090-6371-0) / 10 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA090037 |
FDA SPL set id | 826332 |
Labeler | A-S Medication Solutions |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2009-07-14 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 50090-6371 |
NDC Item 50090681400
NDC 9 | 50090-6814 |
---|---|
NDC 10 | 50090-6814-0 |
NDC Item | 50090681400 |
Packaging | 1 BOTTLE in 1 CARTON (50090-6814-0) / 10 mL in 1 BOTTLE |
ANDA | ANDA204777 |
COLORTEXT | white(colorless to nearly colorless) |
Color | C48325 __ |
FDA SPL set id | 746492 |
Labeler | A-S Medication Solutions |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2020-06-15 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 50090-6814 |
NDC Item 50383023310
NDC 9 | 50383-233 |
---|---|
NDC 10 | 50383-233-10 |
NDC Item | 50383023310 |
Packaging | 1 BOTTLE, DROPPER in 1 BOX (50383-233-10) / 10 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA077847 |
FDA SPL set id | 640641 |
Labeler | Akorn Operating Company LLC (dba Akorn) |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2008-10-28 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 50383-233 |
NDC Item 60429011510
NDC 9 | 60429-115 |
---|---|
NDC 10 | 60429-115-10 |
NDC Item | 60429011510 |
Packaging | 1 BOTTLE, DROPPER in 1 BOX (60429-115-10) / 10 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA077847 |
FDA SPL set id | 767171 |
Labeler | Golden State Medical Supply, Inc. |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2008-10-28 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 60429-115 |
NDC Item 61314003001
NDC 9 | 61314-030 |
---|---|
NDC 10 | 61314-030-01 |
NDC Item | 61314003001 |
Packaging | 5 mL in 1 BOTTLE (61314-030-01) |
ANDA | ANDA090604 |
FDA SPL set id | 622450 |
Labeler | Sandoz Inc |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2010-01-02 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 61314-030 |
NDC Item 61314003002
NDC 9 | 61314-030 |
---|---|
NDC 10 | 61314-030-02 |
NDC Item | 61314003002 |
Packaging | 10 mL in 1 BOTTLE (61314-030-02) |
ANDA | ANDA090604 |
FDA SPL set id | 622450 |
Labeler | Sandoz Inc |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2010-01-02 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 61314-030 |
NDC Item 62332055310
NDC 9 | 62332-553 |
---|---|
NDC 10 | 62332-553-10 |
NDC Item | 62332055310 |
Packaging | 1 BOTTLE in 1 CARTON (62332-553-10) / 10 mL in 1 BOTTLE |
ANDA | ANDA213099 |
FDA SPL set id | 827411 |
Labeler | Alembic Pharmaceuticals Inc. |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2021-05-04 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 62332-553 |
NDC Item 65862094601
NDC 9 | 65862-946 |
---|---|
NDC 10 | 65862-946-01 |
NDC Item | 65862094601 |
Packaging | 1 BOTTLE, DROPPER in 1 CARTON (65862-946-01) / 10 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA207629 |
FDA SPL set id | 788118 |
Labeler | Aurobindo Pharma Limited |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2021-05-14 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 65862-946 |
NDC Item 68083049001
NDC 9 | 68083-490 |
---|---|
NDC 10 | 68083-490-01 |
NDC Item | 68083049001 |
Packaging | 1 BOTTLE in 1 CARTON (68083-490-01) / 10 mL in 1 BOTTLE |
ANDA | ANDA215520 |
FDA SPL set id | 786662 |
Labeler | Gland Pharma Limited |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2022-09-19 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 68083-490 |
NDC Item 69315030505
NDC 9 | 69315-305 |
---|---|
NDC 10 | 69315-305-05 |
NDC Item | 69315030505 |
Packaging | 1 BOTTLE, PLASTIC in 1 CARTON (69315-305-05) / 5 mL in 1 BOTTLE, PLASTIC |
ANDA | ANDA205295 |
FDA SPL set id | 787995 |
Labeler | Leading Pharma, LLC |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2017-05-18 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 69315-305 |
NDC Item 69315030510
NDC 9 | 69315-305 |
---|---|
NDC 10 | 69315-305-10 |
NDC Item | 69315030510 |
Packaging | 1 BOTTLE, PLASTIC in 1 CARTON (69315-305-10) / 10 mL in 1 BOTTLE, PLASTIC |
ANDA | ANDA205295 |
FDA SPL set id | 787995 |
Labeler | Leading Pharma, LLC |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2017-05-18 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 69315-305 |
NDC Item 70069005101
NDC 9 | 70069-051 |
---|---|
NDC 10 | 70069-051-01 |
NDC Item | 70069005101 |
Packaging | 1 BOTTLE in 1 CARTON (70069-051-01) / 10 mL in 1 BOTTLE |
ANDA | ANDA207523 |
COLORTEXT | WHITE(A clear, colorless to nearly colorless solution) |
Color | C48325 __ |
FDA SPL set id | 755334 |
Labeler | Somerset Therapeutics, LLC |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2019-06-25 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 70069-051 |
NDC Item 70377008211
NDC 9 | 70377-082 |
---|---|
NDC 10 | 70377-082-11 |
NDC Item | 70377008211 |
Packaging | 1 BOTTLE, DISPENSING in 1 CARTON (70377-082-11) / 10 mL in 1 BOTTLE, DISPENSING |
ANDA | ANDA202054 |
FDA SPL set id | 611443 |
Labeler | Biocon Pharma Inc. |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2022-01-08 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 70377-082 |
NDC Item 71921022610
NDC 9 | 71921-226 |
---|---|
NDC 10 | 71921-226-10 |
NDC Item | 71921022610 |
Packaging | 1 BOTTLE, DISPENSING in 1 CARTON (71921-226-10) / 10 mL in 1 BOTTLE, DISPENSING |
ANDA | ANDA202054 |
FDA SPL set id | 724181 |
Labeler | Florida Pharmaceutical Products, LLC |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2023-08-16 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 71921-226 |
NDC Item 72162216602
NDC 9 | 72162-2166 |
---|---|
NDC 10 | 72162-2166-2 |
NDC Item | 72162216602 |
Packaging | 1 BOTTLE, DROPPER in 1 CARTON (72162-2166-2) / 10 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA090037 |
FDA SPL set id | 752883 |
Labeler | Bryant Ranch Prepack |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2009-07-14 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 72162-2166 |
NDC Item 72162218402
NDC 9 | 72162-2184 |
---|---|
NDC 10 | 72162-2184-2 |
NDC Item | 72162218402 |
Packaging | 10 mL in 1 BOTTLE (72162-2184-2) |
ANDA | ANDA090604 |
FDA SPL set id | 753279 |
Labeler | Bryant Ranch Prepack |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2010-01-02 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 72162-2184 |
NDC Item 72162238102
NDC 9 | 72162-2381 |
---|---|
NDC 10 | 72162-2381-2 |
NDC Item | 72162238102 |
Packaging | 1 BOTTLE in 1 CARTON (72162-2381-2) / 10 mL in 1 BOTTLE |
ANDA | ANDA204777 |
COLORTEXT | white(colorless to nearly colorless) |
Color | C48325 __ |
FDA SPL set id | 815591 |
Labeler | Bryant Ranch Prepack |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2020-06-15 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 72162-2381 |
NDC Item 00527176373
NDC 9 | 0527-1763 |
---|---|
NDC 10 | 0527-1763-73 |
NDC Item | 00527176373 |
Packaging | 1 BOTTLE, DROPPER in 1 CARTON (0527-1763-73) / 10 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA201998 |
FDA SPL set id | 447745 |
Labeler | Lannett Company, Inc. |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2014-12-17 |
Marketing status | COMPLETED |
Related queries | Properties for NDC 9 0527-1763 |
NDC Item 00781605470
NDC 9 | 0781-6054 |
---|---|
NDC 10 | 0781-6054-70 |
NDC Item | 00781605470 |
Packaging | 1 BOTTLE, DROPPER in 1 CARTON (0781-6054-70) / 10 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA077847 |
Labeler | Sandoz Inc |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing status | COMPLETED |
Related queries | Properties for NDC 9 0781-6054 |
NDC Item 14445040510
NDC 9 | 14445-405 |
---|---|
NDC 10 | 14445-405-10 |
NDC Item | 14445040510 |
Packaging | 1 BOTTLE, DISPENSING in 1 CARTON (14445-405-10) / 10 mL in 1 BOTTLE, DISPENSING |
ANDA | ANDA202054 |
FDA SPL set id | 837670 |
Labeler | Indoco Remedies Limited |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2021-05-14 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 14445-405 |
NDC Item 24208048605
NDC 9 | 24208-486 |
---|---|
NDC 10 | 24208-486-05 |
NDC Item | 24208048605 |
Packaging | 1 BOTTLE, DROPPER in 1 CARTON (24208-486-05) / 5 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA090037 |
FDA SPL set id | 744119 |
Labeler | Bausch & Lomb Incorporated |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2009-07-14 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 24208-486 |
NDC Item 24208048610
NDC 9 | 24208-486 |
---|---|
NDC 10 | 24208-486-10 |
NDC Item | 24208048610 |
Packaging | 1 BOTTLE, DROPPER in 1 CARTON (24208-486-10) / 10 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA090037 |
FDA SPL set id | 744119 |
Labeler | Bausch & Lomb Incorporated |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2009-07-14 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 24208-486 |
NDC Item 42571014726
NDC 9 | 42571-147 |
---|---|
NDC 10 | 42571-147-26 |
NDC Item | 42571014726 |
Packaging | 1 BOTTLE in 1 CARTON (42571-147-26) / 10 mL in 1 BOTTLE |
ANDA | ANDA204777 |
COLORTEXT | white(colorless to nearly colorless) |
Color | C48325 __ |
FDA SPL set id | 812624 |
Labeler | Micro Labs Limited |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2020-06-15 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 42571-147 |
NDC Item 46708055310
NDC 9 | 46708-553 |
---|---|
NDC 10 | 46708-553-10 |
NDC Item | 46708055310 |
Packaging | 1 BOTTLE in 1 CARTON (46708-553-10) / 10 mL in 1 BOTTLE |
ANDA | ANDA213099 |
FDA SPL set id | 827356 |
Labeler | Alembic Pharmaceuticals Limited |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2021-05-04 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 46708-553 |
NDC Item 50090286700
NDC 9 | 50090-2867 |
---|---|
NDC 10 | 50090-2867-0 |
NDC Item | 50090286700 |
Packaging | 1 BOTTLE, DISPENSING in 1 CARTON (50090-2867-0) / 10 mL in 1 BOTTLE, DISPENSING |
ANDA | ANDA202054 |
FDA SPL set id | 302402 |
Labeler | A-S Medication Solutions LLC |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2015-02-17 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 50090-2867 |
NDC Item 50090637100
NDC 9 | 50090-6371 |
---|---|
NDC 10 | 50090-6371-0 |
NDC Item | 50090637100 |
Packaging | 1 BOTTLE, DROPPER in 1 CARTON (50090-6371-0) / 10 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA090037 |
FDA SPL set id | 826332 |
Labeler | A-S Medication Solutions |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2009-07-14 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 50090-6371 |
NDC Item 50090681400
NDC 9 | 50090-6814 |
---|---|
NDC 10 | 50090-6814-0 |
NDC Item | 50090681400 |
Packaging | 1 BOTTLE in 1 CARTON (50090-6814-0) / 10 mL in 1 BOTTLE |
ANDA | ANDA204777 |
COLORTEXT | white(colorless to nearly colorless) |
Color | C48325 __ |
FDA SPL set id | 746492 |
Labeler | A-S Medication Solutions |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2020-06-15 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 50090-6814 |
NDC Item 50383023310
NDC 9 | 50383-233 |
---|---|
NDC 10 | 50383-233-10 |
NDC Item | 50383023310 |
Packaging | 1 BOTTLE, DROPPER in 1 BOX (50383-233-10) / 10 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA077847 |
FDA SPL set id | 640641 |
Labeler | Akorn Operating Company LLC (dba Akorn) |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2008-10-28 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 50383-233 |
NDC Item 60429011510
NDC 9 | 60429-115 |
---|---|
NDC 10 | 60429-115-10 |
NDC Item | 60429011510 |
Packaging | 1 BOTTLE, DROPPER in 1 BOX (60429-115-10) / 10 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA077847 |
FDA SPL set id | 767171 |
Labeler | Golden State Medical Supply, Inc. |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2008-10-28 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 60429-115 |
NDC Item 61314003001
NDC 9 | 61314-030 |
---|---|
NDC 10 | 61314-030-01 |
NDC Item | 61314003001 |
Packaging | 5 mL in 1 BOTTLE (61314-030-01) |
ANDA | ANDA090604 |
FDA SPL set id | 622450 |
Labeler | Sandoz Inc |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2010-01-02 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 61314-030 |
NDC Item 61314003002
NDC 9 | 61314-030 |
---|---|
NDC 10 | 61314-030-02 |
NDC Item | 61314003002 |
Packaging | 10 mL in 1 BOTTLE (61314-030-02) |
ANDA | ANDA090604 |
FDA SPL set id | 622450 |
Labeler | Sandoz Inc |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2010-01-02 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 61314-030 |
NDC Item 62332055310
NDC 9 | 62332-553 |
---|---|
NDC 10 | 62332-553-10 |
NDC Item | 62332055310 |
Packaging | 1 BOTTLE in 1 CARTON (62332-553-10) / 10 mL in 1 BOTTLE |
ANDA | ANDA213099 |
FDA SPL set id | 827411 |
Labeler | Alembic Pharmaceuticals Inc. |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2021-05-04 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 62332-553 |
NDC Item 65862094601
NDC 9 | 65862-946 |
---|---|
NDC 10 | 65862-946-01 |
NDC Item | 65862094601 |
Packaging | 1 BOTTLE, DROPPER in 1 CARTON (65862-946-01) / 10 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA207629 |
FDA SPL set id | 788118 |
Labeler | Aurobindo Pharma Limited |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2021-05-14 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 65862-946 |
NDC Item 68083049001
NDC 9 | 68083-490 |
---|---|
NDC 10 | 68083-490-01 |
NDC Item | 68083049001 |
Packaging | 1 BOTTLE in 1 CARTON (68083-490-01) / 10 mL in 1 BOTTLE |
ANDA | ANDA215520 |
FDA SPL set id | 786662 |
Labeler | Gland Pharma Limited |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2022-09-19 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 68083-490 |
NDC Item 69315030505
NDC 9 | 69315-305 |
---|---|
NDC 10 | 69315-305-05 |
NDC Item | 69315030505 |
Packaging | 1 BOTTLE, PLASTIC in 1 CARTON (69315-305-05) / 5 mL in 1 BOTTLE, PLASTIC |
ANDA | ANDA205295 |
FDA SPL set id | 787995 |
Labeler | Leading Pharma, LLC |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2017-05-18 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 69315-305 |
NDC Item 69315030510
NDC 9 | 69315-305 |
---|---|
NDC 10 | 69315-305-10 |
NDC Item | 69315030510 |
Packaging | 1 BOTTLE, PLASTIC in 1 CARTON (69315-305-10) / 10 mL in 1 BOTTLE, PLASTIC |
ANDA | ANDA205295 |
FDA SPL set id | 787995 |
Labeler | Leading Pharma, LLC |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2017-05-18 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 69315-305 |
NDC Item 70069005101
NDC 9 | 70069-051 |
---|---|
NDC 10 | 70069-051-01 |
NDC Item | 70069005101 |
Packaging | 1 BOTTLE in 1 CARTON (70069-051-01) / 10 mL in 1 BOTTLE |
ANDA | ANDA207523 |
COLORTEXT | WHITE(A clear, colorless to nearly colorless solution) |
Color | C48325 __ |
FDA SPL set id | 755334 |
Labeler | Somerset Therapeutics, LLC |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2019-06-25 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 70069-051 |
NDC Item 70377008211
NDC 9 | 70377-082 |
---|---|
NDC 10 | 70377-082-11 |
NDC Item | 70377008211 |
Packaging | 1 BOTTLE, DISPENSING in 1 CARTON (70377-082-11) / 10 mL in 1 BOTTLE, DISPENSING |
ANDA | ANDA202054 |
FDA SPL set id | 611443 |
Labeler | Biocon Pharma Inc. |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2022-01-08 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 70377-082 |
NDC Item 71921022610
NDC 9 | 71921-226 |
---|---|
NDC 10 | 71921-226-10 |
NDC Item | 71921022610 |
Packaging | 1 BOTTLE, DISPENSING in 1 CARTON (71921-226-10) / 10 mL in 1 BOTTLE, DISPENSING |
ANDA | ANDA202054 |
FDA SPL set id | 724181 |
Labeler | Florida Pharmaceutical Products, LLC |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2023-08-16 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 71921-226 |
NDC Item 72162216602
NDC 9 | 72162-2166 |
---|---|
NDC 10 | 72162-2166-2 |
NDC Item | 72162216602 |
Packaging | 1 BOTTLE, DROPPER in 1 CARTON (72162-2166-2) / 10 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA090037 |
FDA SPL set id | 752883 |
Labeler | Bryant Ranch Prepack |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2009-07-14 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 72162-2166 |
NDC Item 72162218402
NDC 9 | 72162-2184 |
---|---|
NDC 10 | 72162-2184-2 |
NDC Item | 72162218402 |
Packaging | 10 mL in 1 BOTTLE (72162-2184-2) |
ANDA | ANDA090604 |
FDA SPL set id | 753279 |
Labeler | Bryant Ranch Prepack |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2010-01-02 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 72162-2184 |
NDC Item 72162238102
NDC 9 | 72162-2381 |
---|---|
NDC 10 | 72162-2381-2 |
NDC Item | 72162238102 |
Packaging | 1 BOTTLE in 1 CARTON (72162-2381-2) / 10 mL in 1 BOTTLE |
ANDA | ANDA204777 |
COLORTEXT | white(colorless to nearly colorless) |
Color | C48325 __ |
FDA SPL set id | 815591 |
Labeler | Bryant Ranch Prepack |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2020-06-15 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 72162-2381 |
NDC Item 00527176373
NDC 9 | 0527-1763 |
---|---|
NDC 10 | 0527-1763-73 |
NDC Item | 00527176373 |
Packaging | 1 BOTTLE, DROPPER in 1 CARTON (0527-1763-73) / 10 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA201998 |
FDA SPL set id | 447745 |
Labeler | Lannett Company, Inc. |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2014-12-17 |
Marketing status | COMPLETED |
Related queries | Properties for NDC 9 0527-1763 |
NDC Item 00781605470
NDC 9 | 0781-6054 |
---|---|
NDC 10 | 0781-6054-70 |
NDC Item | 00781605470 |
Packaging | 1 BOTTLE, DROPPER in 1 CARTON (0781-6054-70) / 10 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA077847 |
Labeler | Sandoz Inc |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing status | COMPLETED |
Related queries | Properties for NDC 9 0781-6054 |
NDC Item 14445040510
NDC 9 | 14445-405 |
---|---|
NDC 10 | 14445-405-10 |
NDC Item | 14445040510 |
Packaging | 1 BOTTLE, DISPENSING in 1 CARTON (14445-405-10) / 10 mL in 1 BOTTLE, DISPENSING |
ANDA | ANDA202054 |
FDA SPL set id | 837670 |
Labeler | Indoco Remedies Limited |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2021-05-14 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 14445-405 |
NDC Item 24208048605
NDC 9 | 24208-486 |
---|---|
NDC 10 | 24208-486-05 |
NDC Item | 24208048605 |
Packaging | 1 BOTTLE, DROPPER in 1 CARTON (24208-486-05) / 5 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA090037 |
FDA SPL set id | 744119 |
Labeler | Bausch & Lomb Incorporated |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2009-07-14 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 24208-486 |
NDC Item 24208048610
NDC 9 | 24208-486 |
---|---|
NDC 10 | 24208-486-10 |
NDC Item | 24208048610 |
Packaging | 1 BOTTLE, DROPPER in 1 CARTON (24208-486-10) / 10 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA090037 |
FDA SPL set id | 744119 |
Labeler | Bausch & Lomb Incorporated |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2009-07-14 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 24208-486 |
NDC Item 42571014726
NDC 9 | 42571-147 |
---|---|
NDC 10 | 42571-147-26 |
NDC Item | 42571014726 |
Packaging | 1 BOTTLE in 1 CARTON (42571-147-26) / 10 mL in 1 BOTTLE |
ANDA | ANDA204777 |
COLORTEXT | white(colorless to nearly colorless) |
Color | C48325 __ |
FDA SPL set id | 812624 |
Labeler | Micro Labs Limited |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2020-06-15 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 42571-147 |
NDC Item 46708055310
NDC 9 | 46708-553 |
---|---|
NDC 10 | 46708-553-10 |
NDC Item | 46708055310 |
Packaging | 1 BOTTLE in 1 CARTON (46708-553-10) / 10 mL in 1 BOTTLE |
ANDA | ANDA213099 |
FDA SPL set id | 827356 |
Labeler | Alembic Pharmaceuticals Limited |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2021-05-04 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 46708-553 |
NDC Item 50090286700
NDC 9 | 50090-2867 |
---|---|
NDC 10 | 50090-2867-0 |
NDC Item | 50090286700 |
Packaging | 1 BOTTLE, DISPENSING in 1 CARTON (50090-2867-0) / 10 mL in 1 BOTTLE, DISPENSING |
ANDA | ANDA202054 |
FDA SPL set id | 302402 |
Labeler | A-S Medication Solutions LLC |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2015-02-17 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 50090-2867 |
NDC Item 50090637100
NDC 9 | 50090-6371 |
---|---|
NDC 10 | 50090-6371-0 |
NDC Item | 50090637100 |
Packaging | 1 BOTTLE, DROPPER in 1 CARTON (50090-6371-0) / 10 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA090037 |
FDA SPL set id | 826332 |
Labeler | A-S Medication Solutions |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2009-07-14 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 50090-6371 |
NDC Item 50090681400
NDC 9 | 50090-6814 |
---|---|
NDC 10 | 50090-6814-0 |
NDC Item | 50090681400 |
Packaging | 1 BOTTLE in 1 CARTON (50090-6814-0) / 10 mL in 1 BOTTLE |
ANDA | ANDA204777 |
COLORTEXT | white(colorless to nearly colorless) |
Color | C48325 __ |
FDA SPL set id | 746492 |
Labeler | A-S Medication Solutions |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2020-06-15 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 50090-6814 |
NDC Item 50383023310
NDC 9 | 50383-233 |
---|---|
NDC 10 | 50383-233-10 |
NDC Item | 50383023310 |
Packaging | 1 BOTTLE, DROPPER in 1 BOX (50383-233-10) / 10 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA077847 |
FDA SPL set id | 640641 |
Labeler | Akorn Operating Company LLC (dba Akorn) |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2008-10-28 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 50383-233 |
NDC Item 60429011510
NDC 9 | 60429-115 |
---|---|
NDC 10 | 60429-115-10 |
NDC Item | 60429011510 |
Packaging | 1 BOTTLE, DROPPER in 1 BOX (60429-115-10) / 10 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA077847 |
FDA SPL set id | 767171 |
Labeler | Golden State Medical Supply, Inc. |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2008-10-28 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 60429-115 |
NDC Item 61314003001
NDC 9 | 61314-030 |
---|---|
NDC 10 | 61314-030-01 |
NDC Item | 61314003001 |
Packaging | 5 mL in 1 BOTTLE (61314-030-01) |
ANDA | ANDA090604 |
FDA SPL set id | 622450 |
Labeler | Sandoz Inc |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2010-01-02 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 61314-030 |
NDC Item 61314003002
NDC 9 | 61314-030 |
---|---|
NDC 10 | 61314-030-02 |
NDC Item | 61314003002 |
Packaging | 10 mL in 1 BOTTLE (61314-030-02) |
ANDA | ANDA090604 |
FDA SPL set id | 622450 |
Labeler | Sandoz Inc |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2010-01-02 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 61314-030 |
NDC Item 62332055310
NDC 9 | 62332-553 |
---|---|
NDC 10 | 62332-553-10 |
NDC Item | 62332055310 |
Packaging | 1 BOTTLE in 1 CARTON (62332-553-10) / 10 mL in 1 BOTTLE |
ANDA | ANDA213099 |
FDA SPL set id | 827411 |
Labeler | Alembic Pharmaceuticals Inc. |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2021-05-04 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 62332-553 |
NDC Item 65862094601
NDC 9 | 65862-946 |
---|---|
NDC 10 | 65862-946-01 |
NDC Item | 65862094601 |
Packaging | 1 BOTTLE, DROPPER in 1 CARTON (65862-946-01) / 10 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA207629 |
FDA SPL set id | 788118 |
Labeler | Aurobindo Pharma Limited |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2021-05-14 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 65862-946 |
NDC Item 68083049001
NDC 9 | 68083-490 |
---|---|
NDC 10 | 68083-490-01 |
NDC Item | 68083049001 |
Packaging | 1 BOTTLE in 1 CARTON (68083-490-01) / 10 mL in 1 BOTTLE |
ANDA | ANDA215520 |
FDA SPL set id | 786662 |
Labeler | Gland Pharma Limited |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2022-09-19 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 68083-490 |
NDC Item 69315030505
NDC 9 | 69315-305 |
---|---|
NDC 10 | 69315-305-05 |
NDC Item | 69315030505 |
Packaging | 1 BOTTLE, PLASTIC in 1 CARTON (69315-305-05) / 5 mL in 1 BOTTLE, PLASTIC |
ANDA | ANDA205295 |
FDA SPL set id | 787995 |
Labeler | Leading Pharma, LLC |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2017-05-18 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 69315-305 |
NDC Item 69315030510
NDC 9 | 69315-305 |
---|---|
NDC 10 | 69315-305-10 |
NDC Item | 69315030510 |
Packaging | 1 BOTTLE, PLASTIC in 1 CARTON (69315-305-10) / 10 mL in 1 BOTTLE, PLASTIC |
ANDA | ANDA205295 |
FDA SPL set id | 787995 |
Labeler | Leading Pharma, LLC |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2017-05-18 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 69315-305 |
NDC Item 70069005101
NDC 9 | 70069-051 |
---|---|
NDC 10 | 70069-051-01 |
NDC Item | 70069005101 |
Packaging | 1 BOTTLE in 1 CARTON (70069-051-01) / 10 mL in 1 BOTTLE |
ANDA | ANDA207523 |
COLORTEXT | WHITE(A clear, colorless to nearly colorless solution) |
Color | C48325 __ |
FDA SPL set id | 755334 |
Labeler | Somerset Therapeutics, LLC |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2019-06-25 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 70069-051 |
NDC Item 70377008211
NDC 9 | 70377-082 |
---|---|
NDC 10 | 70377-082-11 |
NDC Item | 70377008211 |
Packaging | 1 BOTTLE, DISPENSING in 1 CARTON (70377-082-11) / 10 mL in 1 BOTTLE, DISPENSING |
ANDA | ANDA202054 |
FDA SPL set id | 611443 |
Labeler | Biocon Pharma Inc. |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2022-01-08 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 70377-082 |
NDC Item 71921022610
NDC 9 | 71921-226 |
---|---|
NDC 10 | 71921-226-10 |
NDC Item | 71921022610 |
Packaging | 1 BOTTLE, DISPENSING in 1 CARTON (71921-226-10) / 10 mL in 1 BOTTLE, DISPENSING |
ANDA | ANDA202054 |
FDA SPL set id | 724181 |
Labeler | Florida Pharmaceutical Products, LLC |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2023-08-16 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 71921-226 |
NDC Item 72162216602
NDC 9 | 72162-2166 |
---|---|
NDC 10 | 72162-2166-2 |
NDC Item | 72162216602 |
Packaging | 1 BOTTLE, DROPPER in 1 CARTON (72162-2166-2) / 10 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA090037 |
FDA SPL set id | 752883 |
Labeler | Bryant Ranch Prepack |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2009-07-14 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 72162-2166 |
NDC Item 72162218402
NDC 9 | 72162-2184 |
---|---|
NDC 10 | 72162-2184-2 |
NDC Item | 72162218402 |
Packaging | 10 mL in 1 BOTTLE (72162-2184-2) |
ANDA | ANDA090604 |
FDA SPL set id | 753279 |
Labeler | Bryant Ranch Prepack |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2010-01-02 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 72162-2184 |
NDC Item 72162238102
NDC 9 | 72162-2381 |
---|---|
NDC 10 | 72162-2381-2 |
NDC Item | 72162238102 |
Packaging | 1 BOTTLE in 1 CARTON (72162-2381-2) / 10 mL in 1 BOTTLE |
ANDA | ANDA204777 |
COLORTEXT | white(colorless to nearly colorless) |
Color | C48325 __ |
FDA SPL set id | 815591 |
Labeler | Bryant Ranch Prepack |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2020-06-15 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 72162-2381 |
NDC Item 00527176373
NDC 9 | 0527-1763 |
---|---|
NDC 10 | 0527-1763-73 |
NDC Item | 00527176373 |
Packaging | 1 BOTTLE, DROPPER in 1 CARTON (0527-1763-73) / 10 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA201998 |
FDA SPL set id | 447745 |
Labeler | Lannett Company, Inc. |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2014-12-17 |
Marketing status | COMPLETED |
Related queries | Properties for NDC 9 0527-1763 |
NDC Item 00781605470
NDC 9 | 0781-6054 |
---|---|
NDC 10 | 0781-6054-70 |
NDC Item | 00781605470 |
Packaging | 1 BOTTLE, DROPPER in 1 CARTON (0781-6054-70) / 10 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA077847 |
Labeler | Sandoz Inc |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing status | COMPLETED |
Related queries | Properties for NDC 9 0781-6054 |
NDC Item 14445040510
NDC 9 | 14445-405 |
---|---|
NDC 10 | 14445-405-10 |
NDC Item | 14445040510 |
Packaging | 1 BOTTLE, DISPENSING in 1 CARTON (14445-405-10) / 10 mL in 1 BOTTLE, DISPENSING |
ANDA | ANDA202054 |
FDA SPL set id | 837670 |
Labeler | Indoco Remedies Limited |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2021-05-14 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 14445-405 |
NDC Item 24208048605
NDC 9 | 24208-486 |
---|---|
NDC 10 | 24208-486-05 |
NDC Item | 24208048605 |
Packaging | 1 BOTTLE, DROPPER in 1 CARTON (24208-486-05) / 5 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA090037 |
FDA SPL set id | 744119 |
Labeler | Bausch & Lomb Incorporated |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2009-07-14 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 24208-486 |
NDC Item 24208048610
NDC 9 | 24208-486 |
---|---|
NDC 10 | 24208-486-10 |
NDC Item | 24208048610 |
Packaging | 1 BOTTLE, DROPPER in 1 CARTON (24208-486-10) / 10 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA090037 |
FDA SPL set id | 744119 |
Labeler | Bausch & Lomb Incorporated |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2009-07-14 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 24208-486 |
NDC Item 42571014726
NDC 9 | 42571-147 |
---|---|
NDC 10 | 42571-147-26 |
NDC Item | 42571014726 |
Packaging | 1 BOTTLE in 1 CARTON (42571-147-26) / 10 mL in 1 BOTTLE |
ANDA | ANDA204777 |
COLORTEXT | white(colorless to nearly colorless) |
Color | C48325 __ |
FDA SPL set id | 812624 |
Labeler | Micro Labs Limited |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2020-06-15 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 42571-147 |
NDC Item 46708055310
NDC 9 | 46708-553 |
---|---|
NDC 10 | 46708-553-10 |
NDC Item | 46708055310 |
Packaging | 1 BOTTLE in 1 CARTON (46708-553-10) / 10 mL in 1 BOTTLE |
ANDA | ANDA213099 |
FDA SPL set id | 827356 |
Labeler | Alembic Pharmaceuticals Limited |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2021-05-04 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 46708-553 |
NDC Item 50090286700
NDC 9 | 50090-2867 |
---|---|
NDC 10 | 50090-2867-0 |
NDC Item | 50090286700 |
Packaging | 1 BOTTLE, DISPENSING in 1 CARTON (50090-2867-0) / 10 mL in 1 BOTTLE, DISPENSING |
ANDA | ANDA202054 |
FDA SPL set id | 302402 |
Labeler | A-S Medication Solutions LLC |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2015-02-17 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 50090-2867 |
NDC Item 50090637100
NDC 9 | 50090-6371 |
---|---|
NDC 10 | 50090-6371-0 |
NDC Item | 50090637100 |
Packaging | 1 BOTTLE, DROPPER in 1 CARTON (50090-6371-0) / 10 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA090037 |
FDA SPL set id | 826332 |
Labeler | A-S Medication Solutions |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2009-07-14 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 50090-6371 |
NDC Item 50090681400
NDC 9 | 50090-6814 |
---|---|
NDC 10 | 50090-6814-0 |
NDC Item | 50090681400 |
Packaging | 1 BOTTLE in 1 CARTON (50090-6814-0) / 10 mL in 1 BOTTLE |
ANDA | ANDA204777 |
COLORTEXT | white(colorless to nearly colorless) |
Color | C48325 __ |
FDA SPL set id | 746492 |
Labeler | A-S Medication Solutions |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2020-06-15 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 50090-6814 |
NDC Item 50383023310
NDC 9 | 50383-233 |
---|---|
NDC 10 | 50383-233-10 |
NDC Item | 50383023310 |
Packaging | 1 BOTTLE, DROPPER in 1 BOX (50383-233-10) / 10 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA077847 |
FDA SPL set id | 640641 |
Labeler | Akorn Operating Company LLC (dba Akorn) |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2008-10-28 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 50383-233 |
NDC Item 60429011510
NDC 9 | 60429-115 |
---|---|
NDC 10 | 60429-115-10 |
NDC Item | 60429011510 |
Packaging | 1 BOTTLE, DROPPER in 1 BOX (60429-115-10) / 10 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA077847 |
FDA SPL set id | 767171 |
Labeler | Golden State Medical Supply, Inc. |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2008-10-28 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 60429-115 |
NDC Item 61314003001
NDC 9 | 61314-030 |
---|---|
NDC 10 | 61314-030-01 |
NDC Item | 61314003001 |
Packaging | 5 mL in 1 BOTTLE (61314-030-01) |
ANDA | ANDA090604 |
FDA SPL set id | 622450 |
Labeler | Sandoz Inc |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2010-01-02 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 61314-030 |
NDC Item 61314003002
NDC 9 | 61314-030 |
---|---|
NDC 10 | 61314-030-02 |
NDC Item | 61314003002 |
Packaging | 10 mL in 1 BOTTLE (61314-030-02) |
ANDA | ANDA090604 |
FDA SPL set id | 622450 |
Labeler | Sandoz Inc |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2010-01-02 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 61314-030 |
NDC Item 62332055310
NDC 9 | 62332-553 |
---|---|
NDC 10 | 62332-553-10 |
NDC Item | 62332055310 |
Packaging | 1 BOTTLE in 1 CARTON (62332-553-10) / 10 mL in 1 BOTTLE |
ANDA | ANDA213099 |
FDA SPL set id | 827411 |
Labeler | Alembic Pharmaceuticals Inc. |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2021-05-04 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 62332-553 |
NDC Item 65862094601
NDC 9 | 65862-946 |
---|---|
NDC 10 | 65862-946-01 |
NDC Item | 65862094601 |
Packaging | 1 BOTTLE, DROPPER in 1 CARTON (65862-946-01) / 10 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA207629 |
FDA SPL set id | 788118 |
Labeler | Aurobindo Pharma Limited |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2021-05-14 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 65862-946 |
NDC Item 68083049001
NDC 9 | 68083-490 |
---|---|
NDC 10 | 68083-490-01 |
NDC Item | 68083049001 |
Packaging | 1 BOTTLE in 1 CARTON (68083-490-01) / 10 mL in 1 BOTTLE |
ANDA | ANDA215520 |
FDA SPL set id | 786662 |
Labeler | Gland Pharma Limited |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2022-09-19 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 68083-490 |
NDC Item 69315030505
NDC 9 | 69315-305 |
---|---|
NDC 10 | 69315-305-05 |
NDC Item | 69315030505 |
Packaging | 1 BOTTLE, PLASTIC in 1 CARTON (69315-305-05) / 5 mL in 1 BOTTLE, PLASTIC |
ANDA | ANDA205295 |
FDA SPL set id | 787995 |
Labeler | Leading Pharma, LLC |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2017-05-18 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 69315-305 |
NDC Item 69315030510
NDC 9 | 69315-305 |
---|---|
NDC 10 | 69315-305-10 |
NDC Item | 69315030510 |
Packaging | 1 BOTTLE, PLASTIC in 1 CARTON (69315-305-10) / 10 mL in 1 BOTTLE, PLASTIC |
ANDA | ANDA205295 |
FDA SPL set id | 787995 |
Labeler | Leading Pharma, LLC |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2017-05-18 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 69315-305 |
NDC Item 70069005101
NDC 9 | 70069-051 |
---|---|
NDC 10 | 70069-051-01 |
NDC Item | 70069005101 |
Packaging | 1 BOTTLE in 1 CARTON (70069-051-01) / 10 mL in 1 BOTTLE |
ANDA | ANDA207523 |
COLORTEXT | WHITE(A clear, colorless to nearly colorless solution) |
Color | C48325 __ |
FDA SPL set id | 755334 |
Labeler | Somerset Therapeutics, LLC |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2019-06-25 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 70069-051 |
NDC Item 70377008211
NDC 9 | 70377-082 |
---|---|
NDC 10 | 70377-082-11 |
NDC Item | 70377008211 |
Packaging | 1 BOTTLE, DISPENSING in 1 CARTON (70377-082-11) / 10 mL in 1 BOTTLE, DISPENSING |
ANDA | ANDA202054 |
FDA SPL set id | 611443 |
Labeler | Biocon Pharma Inc. |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2022-01-08 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 70377-082 |
NDC Item 71921022610
NDC 9 | 71921-226 |
---|---|
NDC 10 | 71921-226-10 |
NDC Item | 71921022610 |
Packaging | 1 BOTTLE, DISPENSING in 1 CARTON (71921-226-10) / 10 mL in 1 BOTTLE, DISPENSING |
ANDA | ANDA202054 |
FDA SPL set id | 724181 |
Labeler | Florida Pharmaceutical Products, LLC |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2023-08-16 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 71921-226 |
NDC Item 72162216602
NDC 9 | 72162-2166 |
---|---|
NDC 10 | 72162-2166-2 |
NDC Item | 72162216602 |
Packaging | 1 BOTTLE, DROPPER in 1 CARTON (72162-2166-2) / 10 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA090037 |
FDA SPL set id | 752883 |
Labeler | Bryant Ranch Prepack |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2009-07-14 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 72162-2166 |
NDC Item 72162218402
NDC 9 | 72162-2184 |
---|---|
NDC 10 | 72162-2184-2 |
NDC Item | 72162218402 |
Packaging | 10 mL in 1 BOTTLE (72162-2184-2) |
ANDA | ANDA090604 |
FDA SPL set id | 753279 |
Labeler | Bryant Ranch Prepack |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2010-01-02 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 72162-2184 |
NDC Item 72162238102
NDC 9 | 72162-2381 |
---|---|
NDC 10 | 72162-2381-2 |
NDC Item | 72162238102 |
Packaging | 1 BOTTLE in 1 CARTON (72162-2381-2) / 10 mL in 1 BOTTLE |
ANDA | ANDA204777 |
COLORTEXT | white(colorless to nearly colorless) |
Color | C48325 __ |
FDA SPL set id | 815591 |
Labeler | Bryant Ranch Prepack |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2020-06-15 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 72162-2381 |
NDC Item 00527176373
NDC 9 | 0527-1763 |
---|---|
NDC 10 | 0527-1763-73 |
NDC Item | 00527176373 |
Packaging | 1 BOTTLE, DROPPER in 1 CARTON (0527-1763-73) / 10 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA201998 |
FDA SPL set id | 447745 |
Labeler | Lannett Company, Inc. |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2014-12-17 |
Marketing status | COMPLETED |
Related queries | Properties for NDC 9 0527-1763 |
NDC Item 00781605470
NDC 9 | 0781-6054 |
---|---|
NDC 10 | 0781-6054-70 |
NDC Item | 00781605470 |
Packaging | 1 BOTTLE, DROPPER in 1 CARTON (0781-6054-70) / 10 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA077847 |
Labeler | Sandoz Inc |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing status | COMPLETED |
Related queries | Properties for NDC 9 0781-6054 |
NDC Item 14445040510
NDC 9 | 14445-405 |
---|---|
NDC 10 | 14445-405-10 |
NDC Item | 14445040510 |
Packaging | 1 BOTTLE, DISPENSING in 1 CARTON (14445-405-10) / 10 mL in 1 BOTTLE, DISPENSING |
ANDA | ANDA202054 |
FDA SPL set id | 837670 |
Labeler | Indoco Remedies Limited |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2021-05-14 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 14445-405 |
NDC Item 24208048605
NDC 9 | 24208-486 |
---|---|
NDC 10 | 24208-486-05 |
NDC Item | 24208048605 |
Packaging | 1 BOTTLE, DROPPER in 1 CARTON (24208-486-05) / 5 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA090037 |
FDA SPL set id | 744119 |
Labeler | Bausch & Lomb Incorporated |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2009-07-14 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 24208-486 |
NDC Item 24208048610
NDC 9 | 24208-486 |
---|---|
NDC 10 | 24208-486-10 |
NDC Item | 24208048610 |
Packaging | 1 BOTTLE, DROPPER in 1 CARTON (24208-486-10) / 10 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA090037 |
FDA SPL set id | 744119 |
Labeler | Bausch & Lomb Incorporated |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2009-07-14 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 24208-486 |
NDC Item 42571014726
NDC 9 | 42571-147 |
---|---|
NDC 10 | 42571-147-26 |
NDC Item | 42571014726 |
Packaging | 1 BOTTLE in 1 CARTON (42571-147-26) / 10 mL in 1 BOTTLE |
ANDA | ANDA204777 |
COLORTEXT | white(colorless to nearly colorless) |
Color | C48325 __ |
FDA SPL set id | 812624 |
Labeler | Micro Labs Limited |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2020-06-15 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 42571-147 |
NDC Item 46708055310
NDC 9 | 46708-553 |
---|---|
NDC 10 | 46708-553-10 |
NDC Item | 46708055310 |
Packaging | 1 BOTTLE in 1 CARTON (46708-553-10) / 10 mL in 1 BOTTLE |
ANDA | ANDA213099 |
FDA SPL set id | 827356 |
Labeler | Alembic Pharmaceuticals Limited |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2021-05-04 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 46708-553 |
NDC Item 50090286700
NDC 9 | 50090-2867 |
---|---|
NDC 10 | 50090-2867-0 |
NDC Item | 50090286700 |
Packaging | 1 BOTTLE, DISPENSING in 1 CARTON (50090-2867-0) / 10 mL in 1 BOTTLE, DISPENSING |
ANDA | ANDA202054 |
FDA SPL set id | 302402 |
Labeler | A-S Medication Solutions LLC |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2015-02-17 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 50090-2867 |
NDC Item 50090637100
NDC 9 | 50090-6371 |
---|---|
NDC 10 | 50090-6371-0 |
NDC Item | 50090637100 |
Packaging | 1 BOTTLE, DROPPER in 1 CARTON (50090-6371-0) / 10 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA090037 |
FDA SPL set id | 826332 |
Labeler | A-S Medication Solutions |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2009-07-14 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 50090-6371 |
NDC Item 50090681400
NDC 9 | 50090-6814 |
---|---|
NDC 10 | 50090-6814-0 |
NDC Item | 50090681400 |
Packaging | 1 BOTTLE in 1 CARTON (50090-6814-0) / 10 mL in 1 BOTTLE |
ANDA | ANDA204777 |
COLORTEXT | white(colorless to nearly colorless) |
Color | C48325 __ |
FDA SPL set id | 746492 |
Labeler | A-S Medication Solutions |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2020-06-15 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 50090-6814 |
NDC Item 50383023310
NDC 9 | 50383-233 |
---|---|
NDC 10 | 50383-233-10 |
NDC Item | 50383023310 |
Packaging | 1 BOTTLE, DROPPER in 1 BOX (50383-233-10) / 10 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA077847 |
FDA SPL set id | 640641 |
Labeler | Akorn Operating Company LLC (dba Akorn) |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2008-10-28 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 50383-233 |
NDC Item 60429011510
NDC 9 | 60429-115 |
---|---|
NDC 10 | 60429-115-10 |
NDC Item | 60429011510 |
Packaging | 1 BOTTLE, DROPPER in 1 BOX (60429-115-10) / 10 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA077847 |
FDA SPL set id | 767171 |
Labeler | Golden State Medical Supply, Inc. |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2008-10-28 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 60429-115 |
NDC Item 61314003001
NDC 9 | 61314-030 |
---|---|
NDC 10 | 61314-030-01 |
NDC Item | 61314003001 |
Packaging | 5 mL in 1 BOTTLE (61314-030-01) |
ANDA | ANDA090604 |
FDA SPL set id | 622450 |
Labeler | Sandoz Inc |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2010-01-02 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 61314-030 |
NDC Item 61314003002
NDC 9 | 61314-030 |
---|---|
NDC 10 | 61314-030-02 |
NDC Item | 61314003002 |
Packaging | 10 mL in 1 BOTTLE (61314-030-02) |
ANDA | ANDA090604 |
FDA SPL set id | 622450 |
Labeler | Sandoz Inc |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2010-01-02 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 61314-030 |
NDC Item 62332055310
NDC 9 | 62332-553 |
---|---|
NDC 10 | 62332-553-10 |
NDC Item | 62332055310 |
Packaging | 1 BOTTLE in 1 CARTON (62332-553-10) / 10 mL in 1 BOTTLE |
ANDA | ANDA213099 |
FDA SPL set id | 827411 |
Labeler | Alembic Pharmaceuticals Inc. |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2021-05-04 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 62332-553 |
NDC Item 65862094601
NDC 9 | 65862-946 |
---|---|
NDC 10 | 65862-946-01 |
NDC Item | 65862094601 |
Packaging | 1 BOTTLE, DROPPER in 1 CARTON (65862-946-01) / 10 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA207629 |
FDA SPL set id | 788118 |
Labeler | Aurobindo Pharma Limited |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2021-05-14 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 65862-946 |
NDC Item 68083049001
NDC 9 | 68083-490 |
---|---|
NDC 10 | 68083-490-01 |
NDC Item | 68083049001 |
Packaging | 1 BOTTLE in 1 CARTON (68083-490-01) / 10 mL in 1 BOTTLE |
ANDA | ANDA215520 |
FDA SPL set id | 786662 |
Labeler | Gland Pharma Limited |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2022-09-19 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 68083-490 |
NDC Item 69315030505
NDC 9 | 69315-305 |
---|---|
NDC 10 | 69315-305-05 |
NDC Item | 69315030505 |
Packaging | 1 BOTTLE, PLASTIC in 1 CARTON (69315-305-05) / 5 mL in 1 BOTTLE, PLASTIC |
ANDA | ANDA205295 |
FDA SPL set id | 787995 |
Labeler | Leading Pharma, LLC |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2017-05-18 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 69315-305 |
NDC Item 69315030510
NDC 9 | 69315-305 |
---|---|
NDC 10 | 69315-305-10 |
NDC Item | 69315030510 |
Packaging | 1 BOTTLE, PLASTIC in 1 CARTON (69315-305-10) / 10 mL in 1 BOTTLE, PLASTIC |
ANDA | ANDA205295 |
FDA SPL set id | 787995 |
Labeler | Leading Pharma, LLC |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2017-05-18 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 69315-305 |
NDC Item 70069005101
NDC 9 | 70069-051 |
---|---|
NDC 10 | 70069-051-01 |
NDC Item | 70069005101 |
Packaging | 1 BOTTLE in 1 CARTON (70069-051-01) / 10 mL in 1 BOTTLE |
ANDA | ANDA207523 |
COLORTEXT | WHITE(A clear, colorless to nearly colorless solution) |
Color | C48325 __ |
FDA SPL set id | 755334 |
Labeler | Somerset Therapeutics, LLC |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2019-06-25 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 70069-051 |
NDC Item 70377008211
NDC 9 | 70377-082 |
---|---|
NDC 10 | 70377-082-11 |
NDC Item | 70377008211 |
Packaging | 1 BOTTLE, DISPENSING in 1 CARTON (70377-082-11) / 10 mL in 1 BOTTLE, DISPENSING |
ANDA | ANDA202054 |
FDA SPL set id | 611443 |
Labeler | Biocon Pharma Inc. |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2022-01-08 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 70377-082 |
NDC Item 71921022610
NDC 9 | 71921-226 |
---|---|
NDC 10 | 71921-226-10 |
NDC Item | 71921022610 |
Packaging | 1 BOTTLE, DISPENSING in 1 CARTON (71921-226-10) / 10 mL in 1 BOTTLE, DISPENSING |
ANDA | ANDA202054 |
FDA SPL set id | 724181 |
Labeler | Florida Pharmaceutical Products, LLC |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2023-08-16 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 71921-226 |
NDC Item 72162216602
NDC 9 | 72162-2166 |
---|---|
NDC 10 | 72162-2166-2 |
NDC Item | 72162216602 |
Packaging | 1 BOTTLE, DROPPER in 1 CARTON (72162-2166-2) / 10 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA090037 |
FDA SPL set id | 752883 |
Labeler | Bryant Ranch Prepack |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2009-07-14 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 72162-2166 |
NDC Item 72162218402
NDC 9 | 72162-2184 |
---|---|
NDC 10 | 72162-2184-2 |
NDC Item | 72162218402 |
Packaging | 10 mL in 1 BOTTLE (72162-2184-2) |
ANDA | ANDA090604 |
FDA SPL set id | 753279 |
Labeler | Bryant Ranch Prepack |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2010-01-02 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 72162-2184 |
NDC Item 72162238102
NDC 9 | 72162-2381 |
---|---|
NDC 10 | 72162-2381-2 |
NDC Item | 72162238102 |
Packaging | 1 BOTTLE in 1 CARTON (72162-2381-2) / 10 mL in 1 BOTTLE |
ANDA | ANDA204777 |
COLORTEXT | white(colorless to nearly colorless) |
Color | C48325 __ |
FDA SPL set id | 815591 |
Labeler | Bryant Ranch Prepack |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2020-06-15 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 72162-2381 |
NDC Item 00527176373
NDC 9 | 0527-1763 |
---|---|
NDC 10 | 0527-1763-73 |
NDC Item | 00527176373 |
Packaging | 1 BOTTLE, DROPPER in 1 CARTON (0527-1763-73) / 10 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA201998 |
FDA SPL set id | 447745 |
Labeler | Lannett Company, Inc. |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2014-12-17 |
Marketing status | COMPLETED |
Related queries | Properties for NDC 9 0527-1763 |
NDC Item 00781605470
NDC 9 | 0781-6054 |
---|---|
NDC 10 | 0781-6054-70 |
NDC Item | 00781605470 |
Packaging | 1 BOTTLE, DROPPER in 1 CARTON (0781-6054-70) / 10 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA077847 |
Labeler | Sandoz Inc |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing status | COMPLETED |
Related queries | Properties for NDC 9 0781-6054 |
NDC Item 14445040510
NDC 9 | 14445-405 |
---|---|
NDC 10 | 14445-405-10 |
NDC Item | 14445040510 |
Packaging | 1 BOTTLE, DISPENSING in 1 CARTON (14445-405-10) / 10 mL in 1 BOTTLE, DISPENSING |
ANDA | ANDA202054 |
FDA SPL set id | 837670 |
Labeler | Indoco Remedies Limited |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2021-05-14 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 14445-405 |
NDC Item 24208048605
NDC 9 | 24208-486 |
---|---|
NDC 10 | 24208-486-05 |
NDC Item | 24208048605 |
Packaging | 1 BOTTLE, DROPPER in 1 CARTON (24208-486-05) / 5 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA090037 |
FDA SPL set id | 744119 |
Labeler | Bausch & Lomb Incorporated |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2009-07-14 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 24208-486 |
NDC Item 24208048610
NDC 9 | 24208-486 |
---|---|
NDC 10 | 24208-486-10 |
NDC Item | 24208048610 |
Packaging | 1 BOTTLE, DROPPER in 1 CARTON (24208-486-10) / 10 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA090037 |
FDA SPL set id | 744119 |
Labeler | Bausch & Lomb Incorporated |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2009-07-14 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 24208-486 |
NDC Item 42571014726
NDC 9 | 42571-147 |
---|---|
NDC 10 | 42571-147-26 |
NDC Item | 42571014726 |
Packaging | 1 BOTTLE in 1 CARTON (42571-147-26) / 10 mL in 1 BOTTLE |
ANDA | ANDA204777 |
COLORTEXT | white(colorless to nearly colorless) |
Color | C48325 __ |
FDA SPL set id | 812624 |
Labeler | Micro Labs Limited |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2020-06-15 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 42571-147 |
NDC Item 46708055310
NDC 9 | 46708-553 |
---|---|
NDC 10 | 46708-553-10 |
NDC Item | 46708055310 |
Packaging | 1 BOTTLE in 1 CARTON (46708-553-10) / 10 mL in 1 BOTTLE |
ANDA | ANDA213099 |
FDA SPL set id | 827356 |
Labeler | Alembic Pharmaceuticals Limited |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2021-05-04 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 46708-553 |
NDC Item 50090286700
NDC 9 | 50090-2867 |
---|---|
NDC 10 | 50090-2867-0 |
NDC Item | 50090286700 |
Packaging | 1 BOTTLE, DISPENSING in 1 CARTON (50090-2867-0) / 10 mL in 1 BOTTLE, DISPENSING |
ANDA | ANDA202054 |
FDA SPL set id | 302402 |
Labeler | A-S Medication Solutions LLC |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2015-02-17 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 50090-2867 |
NDC Item 50090637100
NDC 9 | 50090-6371 |
---|---|
NDC 10 | 50090-6371-0 |
NDC Item | 50090637100 |
Packaging | 1 BOTTLE, DROPPER in 1 CARTON (50090-6371-0) / 10 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA090037 |
FDA SPL set id | 826332 |
Labeler | A-S Medication Solutions |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2009-07-14 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 50090-6371 |
NDC Item 50090681400
NDC 9 | 50090-6814 |
---|---|
NDC 10 | 50090-6814-0 |
NDC Item | 50090681400 |
Packaging | 1 BOTTLE in 1 CARTON (50090-6814-0) / 10 mL in 1 BOTTLE |
ANDA | ANDA204777 |
COLORTEXT | white(colorless to nearly colorless) |
Color | C48325 __ |
FDA SPL set id | 746492 |
Labeler | A-S Medication Solutions |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2020-06-15 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 50090-6814 |
NDC Item 50383023310
NDC 9 | 50383-233 |
---|---|
NDC 10 | 50383-233-10 |
NDC Item | 50383023310 |
Packaging | 1 BOTTLE, DROPPER in 1 BOX (50383-233-10) / 10 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA077847 |
FDA SPL set id | 640641 |
Labeler | Akorn Operating Company LLC (dba Akorn) |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2008-10-28 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 50383-233 |
NDC Item 60429011510
NDC 9 | 60429-115 |
---|---|
NDC 10 | 60429-115-10 |
NDC Item | 60429011510 |
Packaging | 1 BOTTLE, DROPPER in 1 BOX (60429-115-10) / 10 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA077847 |
FDA SPL set id | 767171 |
Labeler | Golden State Medical Supply, Inc. |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2008-10-28 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 60429-115 |
NDC Item 61314003001
NDC 9 | 61314-030 |
---|---|
NDC 10 | 61314-030-01 |
NDC Item | 61314003001 |
Packaging | 5 mL in 1 BOTTLE (61314-030-01) |
ANDA | ANDA090604 |
FDA SPL set id | 622450 |
Labeler | Sandoz Inc |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2010-01-02 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 61314-030 |
NDC Item 61314003002
NDC 9 | 61314-030 |
---|---|
NDC 10 | 61314-030-02 |
NDC Item | 61314003002 |
Packaging | 10 mL in 1 BOTTLE (61314-030-02) |
ANDA | ANDA090604 |
FDA SPL set id | 622450 |
Labeler | Sandoz Inc |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2010-01-02 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 61314-030 |
NDC Item 62332055310
NDC 9 | 62332-553 |
---|---|
NDC 10 | 62332-553-10 |
NDC Item | 62332055310 |
Packaging | 1 BOTTLE in 1 CARTON (62332-553-10) / 10 mL in 1 BOTTLE |
ANDA | ANDA213099 |
FDA SPL set id | 827411 |
Labeler | Alembic Pharmaceuticals Inc. |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2021-05-04 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 62332-553 |
NDC Item 65862094601
NDC 9 | 65862-946 |
---|---|
NDC 10 | 65862-946-01 |
NDC Item | 65862094601 |
Packaging | 1 BOTTLE, DROPPER in 1 CARTON (65862-946-01) / 10 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA207629 |
FDA SPL set id | 788118 |
Labeler | Aurobindo Pharma Limited |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2021-05-14 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 65862-946 |
NDC Item 68083049001
NDC 9 | 68083-490 |
---|---|
NDC 10 | 68083-490-01 |
NDC Item | 68083049001 |
Packaging | 1 BOTTLE in 1 CARTON (68083-490-01) / 10 mL in 1 BOTTLE |
ANDA | ANDA215520 |
FDA SPL set id | 786662 |
Labeler | Gland Pharma Limited |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2022-09-19 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 68083-490 |
NDC Item 69315030505
NDC 9 | 69315-305 |
---|---|
NDC 10 | 69315-305-05 |
NDC Item | 69315030505 |
Packaging | 1 BOTTLE, PLASTIC in 1 CARTON (69315-305-05) / 5 mL in 1 BOTTLE, PLASTIC |
ANDA | ANDA205295 |
FDA SPL set id | 787995 |
Labeler | Leading Pharma, LLC |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2017-05-18 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 69315-305 |
NDC Item 69315030510
NDC 9 | 69315-305 |
---|---|
NDC 10 | 69315-305-10 |
NDC Item | 69315030510 |
Packaging | 1 BOTTLE, PLASTIC in 1 CARTON (69315-305-10) / 10 mL in 1 BOTTLE, PLASTIC |
ANDA | ANDA205295 |
FDA SPL set id | 787995 |
Labeler | Leading Pharma, LLC |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2017-05-18 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 69315-305 |
NDC Item 70069005101
NDC 9 | 70069-051 |
---|---|
NDC 10 | 70069-051-01 |
NDC Item | 70069005101 |
Packaging | 1 BOTTLE in 1 CARTON (70069-051-01) / 10 mL in 1 BOTTLE |
ANDA | ANDA207523 |
COLORTEXT | WHITE(A clear, colorless to nearly colorless solution) |
Color | C48325 __ |
FDA SPL set id | 755334 |
Labeler | Somerset Therapeutics, LLC |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2019-06-25 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 70069-051 |
NDC Item 70377008211
NDC 9 | 70377-082 |
---|---|
NDC 10 | 70377-082-11 |
NDC Item | 70377008211 |
Packaging | 1 BOTTLE, DISPENSING in 1 CARTON (70377-082-11) / 10 mL in 1 BOTTLE, DISPENSING |
ANDA | ANDA202054 |
FDA SPL set id | 611443 |
Labeler | Biocon Pharma Inc. |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2022-01-08 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 70377-082 |
NDC Item 71921022610
NDC 9 | 71921-226 |
---|---|
NDC 10 | 71921-226-10 |
NDC Item | 71921022610 |
Packaging | 1 BOTTLE, DISPENSING in 1 CARTON (71921-226-10) / 10 mL in 1 BOTTLE, DISPENSING |
ANDA | ANDA202054 |
FDA SPL set id | 724181 |
Labeler | Florida Pharmaceutical Products, LLC |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2023-08-16 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 71921-226 |
NDC Item 72162216602
NDC 9 | 72162-2166 |
---|---|
NDC 10 | 72162-2166-2 |
NDC Item | 72162216602 |
Packaging | 1 BOTTLE, DROPPER in 1 CARTON (72162-2166-2) / 10 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA090037 |
FDA SPL set id | 752883 |
Labeler | Bryant Ranch Prepack |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2009-07-14 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 72162-2166 |
NDC Item 72162218402
NDC 9 | 72162-2184 |
---|---|
NDC 10 | 72162-2184-2 |
NDC Item | 72162218402 |
Packaging | 10 mL in 1 BOTTLE (72162-2184-2) |
ANDA | ANDA090604 |
FDA SPL set id | 753279 |
Labeler | Bryant Ranch Prepack |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2010-01-02 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 72162-2184 |
NDC Item 72162238102
NDC 9 | 72162-2381 |
---|---|
NDC 10 | 72162-2381-2 |
NDC Item | 72162238102 |
Packaging | 1 BOTTLE in 1 CARTON (72162-2381-2) / 10 mL in 1 BOTTLE |
ANDA | ANDA204777 |
COLORTEXT | white(colorless to nearly colorless) |
Color | C48325 __ |
FDA SPL set id | 815591 |
Labeler | Bryant Ranch Prepack |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2020-06-15 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 72162-2381 |
NDC Item 00527176373
NDC 9 | 0527-1763 |
---|---|
NDC 10 | 0527-1763-73 |
NDC Item | 00527176373 |
Packaging | 1 BOTTLE, DROPPER in 1 CARTON (0527-1763-73) / 10 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA201998 |
FDA SPL set id | 447745 |
Labeler | Lannett Company, Inc. |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2014-12-17 |
Marketing status | COMPLETED |
Related queries | Properties for NDC 9 0527-1763 |
NDC Item 00781605470
NDC 9 | 0781-6054 |
---|---|
NDC 10 | 0781-6054-70 |
NDC Item | 00781605470 |
Packaging | 1 BOTTLE, DROPPER in 1 CARTON (0781-6054-70) / 10 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA077847 |
Labeler | Sandoz Inc |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing status | COMPLETED |
Related queries | Properties for NDC 9 0781-6054 |
NDC Item 14445040510
NDC 9 | 14445-405 |
---|---|
NDC 10 | 14445-405-10 |
NDC Item | 14445040510 |
Packaging | 1 BOTTLE, DISPENSING in 1 CARTON (14445-405-10) / 10 mL in 1 BOTTLE, DISPENSING |
ANDA | ANDA202054 |
FDA SPL set id | 837670 |
Labeler | Indoco Remedies Limited |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2021-05-14 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 14445-405 |
NDC Item 24208048605
NDC 9 | 24208-486 |
---|---|
NDC 10 | 24208-486-05 |
NDC Item | 24208048605 |
Packaging | 1 BOTTLE, DROPPER in 1 CARTON (24208-486-05) / 5 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA090037 |
FDA SPL set id | 744119 |
Labeler | Bausch & Lomb Incorporated |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2009-07-14 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 24208-486 |
NDC Item 24208048610
NDC 9 | 24208-486 |
---|---|
NDC 10 | 24208-486-10 |
NDC Item | 24208048610 |
Packaging | 1 BOTTLE, DROPPER in 1 CARTON (24208-486-10) / 10 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA090037 |
FDA SPL set id | 744119 |
Labeler | Bausch & Lomb Incorporated |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2009-07-14 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 24208-486 |
NDC Item 42571014726
NDC 9 | 42571-147 |
---|---|
NDC 10 | 42571-147-26 |
NDC Item | 42571014726 |
Packaging | 1 BOTTLE in 1 CARTON (42571-147-26) / 10 mL in 1 BOTTLE |
ANDA | ANDA204777 |
COLORTEXT | white(colorless to nearly colorless) |
Color | C48325 __ |
FDA SPL set id | 812624 |
Labeler | Micro Labs Limited |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2020-06-15 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 42571-147 |
NDC Item 46708055310
NDC 9 | 46708-553 |
---|---|
NDC 10 | 46708-553-10 |
NDC Item | 46708055310 |
Packaging | 1 BOTTLE in 1 CARTON (46708-553-10) / 10 mL in 1 BOTTLE |
ANDA | ANDA213099 |
FDA SPL set id | 827356 |
Labeler | Alembic Pharmaceuticals Limited |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2021-05-04 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 46708-553 |
NDC Item 50090286700
NDC 9 | 50090-2867 |
---|---|
NDC 10 | 50090-2867-0 |
NDC Item | 50090286700 |
Packaging | 1 BOTTLE, DISPENSING in 1 CARTON (50090-2867-0) / 10 mL in 1 BOTTLE, DISPENSING |
ANDA | ANDA202054 |
FDA SPL set id | 302402 |
Labeler | A-S Medication Solutions LLC |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2015-02-17 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 50090-2867 |
NDC Item 50090637100
NDC 9 | 50090-6371 |
---|---|
NDC 10 | 50090-6371-0 |
NDC Item | 50090637100 |
Packaging | 1 BOTTLE, DROPPER in 1 CARTON (50090-6371-0) / 10 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA090037 |
FDA SPL set id | 826332 |
Labeler | A-S Medication Solutions |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2009-07-14 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 50090-6371 |
NDC Item 50090681400
NDC 9 | 50090-6814 |
---|---|
NDC 10 | 50090-6814-0 |
NDC Item | 50090681400 |
Packaging | 1 BOTTLE in 1 CARTON (50090-6814-0) / 10 mL in 1 BOTTLE |
ANDA | ANDA204777 |
COLORTEXT | white(colorless to nearly colorless) |
Color | C48325 __ |
FDA SPL set id | 746492 |
Labeler | A-S Medication Solutions |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2020-06-15 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 50090-6814 |
NDC Item 50383023310
NDC 9 | 50383-233 |
---|---|
NDC 10 | 50383-233-10 |
NDC Item | 50383023310 |
Packaging | 1 BOTTLE, DROPPER in 1 BOX (50383-233-10) / 10 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA077847 |
FDA SPL set id | 640641 |
Labeler | Akorn Operating Company LLC (dba Akorn) |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2008-10-28 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 50383-233 |
NDC Item 60429011510
NDC 9 | 60429-115 |
---|---|
NDC 10 | 60429-115-10 |
NDC Item | 60429011510 |
Packaging | 1 BOTTLE, DROPPER in 1 BOX (60429-115-10) / 10 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA077847 |
FDA SPL set id | 767171 |
Labeler | Golden State Medical Supply, Inc. |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2008-10-28 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 60429-115 |
NDC Item 61314003001
NDC 9 | 61314-030 |
---|---|
NDC 10 | 61314-030-01 |
NDC Item | 61314003001 |
Packaging | 5 mL in 1 BOTTLE (61314-030-01) |
ANDA | ANDA090604 |
FDA SPL set id | 622450 |
Labeler | Sandoz Inc |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2010-01-02 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 61314-030 |
NDC Item 61314003002
NDC 9 | 61314-030 |
---|---|
NDC 10 | 61314-030-02 |
NDC Item | 61314003002 |
Packaging | 10 mL in 1 BOTTLE (61314-030-02) |
ANDA | ANDA090604 |
FDA SPL set id | 622450 |
Labeler | Sandoz Inc |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2010-01-02 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 61314-030 |
NDC Item 62332055310
NDC 9 | 62332-553 |
---|---|
NDC 10 | 62332-553-10 |
NDC Item | 62332055310 |
Packaging | 1 BOTTLE in 1 CARTON (62332-553-10) / 10 mL in 1 BOTTLE |
ANDA | ANDA213099 |
FDA SPL set id | 827411 |
Labeler | Alembic Pharmaceuticals Inc. |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2021-05-04 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 62332-553 |
NDC Item 65862094601
NDC 9 | 65862-946 |
---|---|
NDC 10 | 65862-946-01 |
NDC Item | 65862094601 |
Packaging | 1 BOTTLE, DROPPER in 1 CARTON (65862-946-01) / 10 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA207629 |
FDA SPL set id | 788118 |
Labeler | Aurobindo Pharma Limited |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2021-05-14 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 65862-946 |
NDC Item 68083049001
NDC 9 | 68083-490 |
---|---|
NDC 10 | 68083-490-01 |
NDC Item | 68083049001 |
Packaging | 1 BOTTLE in 1 CARTON (68083-490-01) / 10 mL in 1 BOTTLE |
ANDA | ANDA215520 |
FDA SPL set id | 786662 |
Labeler | Gland Pharma Limited |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2022-09-19 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 68083-490 |
NDC Item 69315030505
NDC 9 | 69315-305 |
---|---|
NDC 10 | 69315-305-05 |
NDC Item | 69315030505 |
Packaging | 1 BOTTLE, PLASTIC in 1 CARTON (69315-305-05) / 5 mL in 1 BOTTLE, PLASTIC |
ANDA | ANDA205295 |
FDA SPL set id | 787995 |
Labeler | Leading Pharma, LLC |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2017-05-18 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 69315-305 |
NDC Item 69315030510
NDC 9 | 69315-305 |
---|---|
NDC 10 | 69315-305-10 |
NDC Item | 69315030510 |
Packaging | 1 BOTTLE, PLASTIC in 1 CARTON (69315-305-10) / 10 mL in 1 BOTTLE, PLASTIC |
ANDA | ANDA205295 |
FDA SPL set id | 787995 |
Labeler | Leading Pharma, LLC |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2017-05-18 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 69315-305 |
NDC Item 70069005101
NDC 9 | 70069-051 |
---|---|
NDC 10 | 70069-051-01 |
NDC Item | 70069005101 |
Packaging | 1 BOTTLE in 1 CARTON (70069-051-01) / 10 mL in 1 BOTTLE |
ANDA | ANDA207523 |
COLORTEXT | WHITE(A clear, colorless to nearly colorless solution) |
Color | C48325 __ |
FDA SPL set id | 755334 |
Labeler | Somerset Therapeutics, LLC |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2019-06-25 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 70069-051 |
NDC Item 70377008211
NDC 9 | 70377-082 |
---|---|
NDC 10 | 70377-082-11 |
NDC Item | 70377008211 |
Packaging | 1 BOTTLE, DISPENSING in 1 CARTON (70377-082-11) / 10 mL in 1 BOTTLE, DISPENSING |
ANDA | ANDA202054 |
FDA SPL set id | 611443 |
Labeler | Biocon Pharma Inc. |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2022-01-08 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 70377-082 |
NDC Item 71921022610
NDC 9 | 71921-226 |
---|---|
NDC 10 | 71921-226-10 |
NDC Item | 71921022610 |
Packaging | 1 BOTTLE, DISPENSING in 1 CARTON (71921-226-10) / 10 mL in 1 BOTTLE, DISPENSING |
ANDA | ANDA202054 |
FDA SPL set id | 724181 |
Labeler | Florida Pharmaceutical Products, LLC |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2023-08-16 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 71921-226 |
NDC Item 72162216602
NDC 9 | 72162-2166 |
---|---|
NDC 10 | 72162-2166-2 |
NDC Item | 72162216602 |
Packaging | 1 BOTTLE, DROPPER in 1 CARTON (72162-2166-2) / 10 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA090037 |
FDA SPL set id | 752883 |
Labeler | Bryant Ranch Prepack |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2009-07-14 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 72162-2166 |
NDC Item 72162218402
NDC 9 | 72162-2184 |
---|---|
NDC 10 | 72162-2184-2 |
NDC Item | 72162218402 |
Packaging | 10 mL in 1 BOTTLE (72162-2184-2) |
ANDA | ANDA090604 |
FDA SPL set id | 753279 |
Labeler | Bryant Ranch Prepack |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2010-01-02 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 72162-2184 |
NDC Item 72162238102
NDC 9 | 72162-2381 |
---|---|
NDC 10 | 72162-2381-2 |
NDC Item | 72162238102 |
Packaging | 1 BOTTLE in 1 CARTON (72162-2381-2) / 10 mL in 1 BOTTLE |
ANDA | ANDA204777 |
COLORTEXT | white(colorless to nearly colorless) |
Color | C48325 __ |
FDA SPL set id | 815591 |
Labeler | Bryant Ranch Prepack |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2020-06-15 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 72162-2381 |
NDC Item 00527176373
NDC 9 | 0527-1763 |
---|---|
NDC 10 | 0527-1763-73 |
NDC Item | 00527176373 |
Packaging | 1 BOTTLE, DROPPER in 1 CARTON (0527-1763-73) / 10 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA201998 |
FDA SPL set id | 447745 |
Labeler | Lannett Company, Inc. |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2014-12-17 |
Marketing status | COMPLETED |
Related queries | Properties for NDC 9 0527-1763 |
NDC Item 00781605470
NDC 9 | 0781-6054 |
---|---|
NDC 10 | 0781-6054-70 |
NDC Item | 00781605470 |
Packaging | 1 BOTTLE, DROPPER in 1 CARTON (0781-6054-70) / 10 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA077847 |
Labeler | Sandoz Inc |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing status | COMPLETED |
Related queries | Properties for NDC 9 0781-6054 |
NDC Item 14445040510
NDC 9 | 14445-405 |
---|---|
NDC 10 | 14445-405-10 |
NDC Item | 14445040510 |
Packaging | 1 BOTTLE, DISPENSING in 1 CARTON (14445-405-10) / 10 mL in 1 BOTTLE, DISPENSING |
ANDA | ANDA202054 |
FDA SPL set id | 837670 |
Labeler | Indoco Remedies Limited |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2021-05-14 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 14445-405 |
NDC Item 24208048605
NDC 9 | 24208-486 |
---|---|
NDC 10 | 24208-486-05 |
NDC Item | 24208048605 |
Packaging | 1 BOTTLE, DROPPER in 1 CARTON (24208-486-05) / 5 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA090037 |
FDA SPL set id | 744119 |
Labeler | Bausch & Lomb Incorporated |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2009-07-14 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 24208-486 |
NDC Item 24208048610
NDC 9 | 24208-486 |
---|---|
NDC 10 | 24208-486-10 |
NDC Item | 24208048610 |
Packaging | 1 BOTTLE, DROPPER in 1 CARTON (24208-486-10) / 10 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA090037 |
FDA SPL set id | 744119 |
Labeler | Bausch & Lomb Incorporated |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2009-07-14 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 24208-486 |
NDC Item 42571014726
NDC 9 | 42571-147 |
---|---|
NDC 10 | 42571-147-26 |
NDC Item | 42571014726 |
Packaging | 1 BOTTLE in 1 CARTON (42571-147-26) / 10 mL in 1 BOTTLE |
ANDA | ANDA204777 |
COLORTEXT | white(colorless to nearly colorless) |
Color | C48325 __ |
FDA SPL set id | 812624 |
Labeler | Micro Labs Limited |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2020-06-15 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 42571-147 |
NDC Item 46708055310
NDC 9 | 46708-553 |
---|---|
NDC 10 | 46708-553-10 |
NDC Item | 46708055310 |
Packaging | 1 BOTTLE in 1 CARTON (46708-553-10) / 10 mL in 1 BOTTLE |
ANDA | ANDA213099 |
FDA SPL set id | 827356 |
Labeler | Alembic Pharmaceuticals Limited |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2021-05-04 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 46708-553 |
NDC Item 50090286700
NDC 9 | 50090-2867 |
---|---|
NDC 10 | 50090-2867-0 |
NDC Item | 50090286700 |
Packaging | 1 BOTTLE, DISPENSING in 1 CARTON (50090-2867-0) / 10 mL in 1 BOTTLE, DISPENSING |
ANDA | ANDA202054 |
FDA SPL set id | 302402 |
Labeler | A-S Medication Solutions LLC |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2015-02-17 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 50090-2867 |
NDC Item 50090637100
NDC 9 | 50090-6371 |
---|---|
NDC 10 | 50090-6371-0 |
NDC Item | 50090637100 |
Packaging | 1 BOTTLE, DROPPER in 1 CARTON (50090-6371-0) / 10 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA090037 |
FDA SPL set id | 826332 |
Labeler | A-S Medication Solutions |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2009-07-14 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 50090-6371 |
NDC Item 50090681400
NDC 9 | 50090-6814 |
---|---|
NDC 10 | 50090-6814-0 |
NDC Item | 50090681400 |
Packaging | 1 BOTTLE in 1 CARTON (50090-6814-0) / 10 mL in 1 BOTTLE |
ANDA | ANDA204777 |
COLORTEXT | white(colorless to nearly colorless) |
Color | C48325 __ |
FDA SPL set id | 746492 |
Labeler | A-S Medication Solutions |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2020-06-15 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 50090-6814 |
NDC Item 50383023310
NDC 9 | 50383-233 |
---|---|
NDC 10 | 50383-233-10 |
NDC Item | 50383023310 |
Packaging | 1 BOTTLE, DROPPER in 1 BOX (50383-233-10) / 10 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA077847 |
FDA SPL set id | 640641 |
Labeler | Akorn Operating Company LLC (dba Akorn) |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2008-10-28 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 50383-233 |
NDC Item 60429011510
NDC 9 | 60429-115 |
---|---|
NDC 10 | 60429-115-10 |
NDC Item | 60429011510 |
Packaging | 1 BOTTLE, DROPPER in 1 BOX (60429-115-10) / 10 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA077847 |
FDA SPL set id | 767171 |
Labeler | Golden State Medical Supply, Inc. |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2008-10-28 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 60429-115 |
NDC Item 61314003001
NDC 9 | 61314-030 |
---|---|
NDC 10 | 61314-030-01 |
NDC Item | 61314003001 |
Packaging | 5 mL in 1 BOTTLE (61314-030-01) |
ANDA | ANDA090604 |
FDA SPL set id | 622450 |
Labeler | Sandoz Inc |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2010-01-02 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 61314-030 |
NDC Item 61314003002
NDC 9 | 61314-030 |
---|---|
NDC 10 | 61314-030-02 |
NDC Item | 61314003002 |
Packaging | 10 mL in 1 BOTTLE (61314-030-02) |
ANDA | ANDA090604 |
FDA SPL set id | 622450 |
Labeler | Sandoz Inc |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2010-01-02 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 61314-030 |
NDC Item 62332055310
NDC 9 | 62332-553 |
---|---|
NDC 10 | 62332-553-10 |
NDC Item | 62332055310 |
Packaging | 1 BOTTLE in 1 CARTON (62332-553-10) / 10 mL in 1 BOTTLE |
ANDA | ANDA213099 |
FDA SPL set id | 827411 |
Labeler | Alembic Pharmaceuticals Inc. |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2021-05-04 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 62332-553 |
NDC Item 65862094601
NDC 9 | 65862-946 |
---|---|
NDC 10 | 65862-946-01 |
NDC Item | 65862094601 |
Packaging | 1 BOTTLE, DROPPER in 1 CARTON (65862-946-01) / 10 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA207629 |
FDA SPL set id | 788118 |
Labeler | Aurobindo Pharma Limited |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2021-05-14 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 65862-946 |
NDC Item 68083049001
NDC 9 | 68083-490 |
---|---|
NDC 10 | 68083-490-01 |
NDC Item | 68083049001 |
Packaging | 1 BOTTLE in 1 CARTON (68083-490-01) / 10 mL in 1 BOTTLE |
ANDA | ANDA215520 |
FDA SPL set id | 786662 |
Labeler | Gland Pharma Limited |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2022-09-19 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 68083-490 |
NDC Item 69315030505
NDC 9 | 69315-305 |
---|---|
NDC 10 | 69315-305-05 |
NDC Item | 69315030505 |
Packaging | 1 BOTTLE, PLASTIC in 1 CARTON (69315-305-05) / 5 mL in 1 BOTTLE, PLASTIC |
ANDA | ANDA205295 |
FDA SPL set id | 787995 |
Labeler | Leading Pharma, LLC |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2017-05-18 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 69315-305 |
NDC Item 69315030510
NDC 9 | 69315-305 |
---|---|
NDC 10 | 69315-305-10 |
NDC Item | 69315030510 |
Packaging | 1 BOTTLE, PLASTIC in 1 CARTON (69315-305-10) / 10 mL in 1 BOTTLE, PLASTIC |
ANDA | ANDA205295 |
FDA SPL set id | 787995 |
Labeler | Leading Pharma, LLC |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2017-05-18 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 69315-305 |
NDC Item 70069005101
NDC 9 | 70069-051 |
---|---|
NDC 10 | 70069-051-01 |
NDC Item | 70069005101 |
Packaging | 1 BOTTLE in 1 CARTON (70069-051-01) / 10 mL in 1 BOTTLE |
ANDA | ANDA207523 |
COLORTEXT | WHITE(A clear, colorless to nearly colorless solution) |
Color | C48325 __ |
FDA SPL set id | 755334 |
Labeler | Somerset Therapeutics, LLC |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2019-06-25 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 70069-051 |
NDC Item 70377008211
NDC 9 | 70377-082 |
---|---|
NDC 10 | 70377-082-11 |
NDC Item | 70377008211 |
Packaging | 1 BOTTLE, DISPENSING in 1 CARTON (70377-082-11) / 10 mL in 1 BOTTLE, DISPENSING |
ANDA | ANDA202054 |
FDA SPL set id | 611443 |
Labeler | Biocon Pharma Inc. |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2022-01-08 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 70377-082 |
NDC Item 71921022610
NDC 9 | 71921-226 |
---|---|
NDC 10 | 71921-226-10 |
NDC Item | 71921022610 |
Packaging | 1 BOTTLE, DISPENSING in 1 CARTON (71921-226-10) / 10 mL in 1 BOTTLE, DISPENSING |
ANDA | ANDA202054 |
FDA SPL set id | 724181 |
Labeler | Florida Pharmaceutical Products, LLC |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2023-08-16 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 71921-226 |
NDC Item 72162216602
NDC 9 | 72162-2166 |
---|---|
NDC 10 | 72162-2166-2 |
NDC Item | 72162216602 |
Packaging | 1 BOTTLE, DROPPER in 1 CARTON (72162-2166-2) / 10 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA090037 |
FDA SPL set id | 752883 |
Labeler | Bryant Ranch Prepack |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2009-07-14 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 72162-2166 |
NDC Item 72162218402
NDC 9 | 72162-2184 |
---|---|
NDC 10 | 72162-2184-2 |
NDC Item | 72162218402 |
Packaging | 10 mL in 1 BOTTLE (72162-2184-2) |
ANDA | ANDA090604 |
FDA SPL set id | 753279 |
Labeler | Bryant Ranch Prepack |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2010-01-02 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 72162-2184 |
NDC Item 72162238102
NDC 9 | 72162-2381 |
---|---|
NDC 10 | 72162-2381-2 |
NDC Item | 72162238102 |
Packaging | 1 BOTTLE in 1 CARTON (72162-2381-2) / 10 mL in 1 BOTTLE |
ANDA | ANDA204777 |
COLORTEXT | white(colorless to nearly colorless) |
Color | C48325 __ |
FDA SPL set id | 815591 |
Labeler | Bryant Ranch Prepack |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2020-06-15 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 72162-2381 |
NDC Item 00527176373
NDC 9 | 0527-1763 |
---|---|
NDC 10 | 0527-1763-73 |
NDC Item | 00527176373 |
Packaging | 1 BOTTLE, DROPPER in 1 CARTON (0527-1763-73) / 10 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA201998 |
FDA SPL set id | 447745 |
Labeler | Lannett Company, Inc. |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2014-12-17 |
Marketing status | COMPLETED |
Related queries | Properties for NDC 9 0527-1763 |
NDC Item 00781605470
NDC 9 | 0781-6054 |
---|---|
NDC 10 | 0781-6054-70 |
NDC Item | 00781605470 |
Packaging | 1 BOTTLE, DROPPER in 1 CARTON (0781-6054-70) / 10 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA077847 |
Labeler | Sandoz Inc |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing status | COMPLETED |
Related queries | Properties for NDC 9 0781-6054 |
NDC Item 14445040510
NDC 9 | 14445-405 |
---|---|
NDC 10 | 14445-405-10 |
NDC Item | 14445040510 |
Packaging | 1 BOTTLE, DISPENSING in 1 CARTON (14445-405-10) / 10 mL in 1 BOTTLE, DISPENSING |
ANDA | ANDA202054 |
FDA SPL set id | 837670 |
Labeler | Indoco Remedies Limited |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2021-05-14 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 14445-405 |
NDC Item 24208048605
NDC 9 | 24208-486 |
---|---|
NDC 10 | 24208-486-05 |
NDC Item | 24208048605 |
Packaging | 1 BOTTLE, DROPPER in 1 CARTON (24208-486-05) / 5 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA090037 |
FDA SPL set id | 744119 |
Labeler | Bausch & Lomb Incorporated |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2009-07-14 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 24208-486 |
NDC Item 24208048610
NDC 9 | 24208-486 |
---|---|
NDC 10 | 24208-486-10 |
NDC Item | 24208048610 |
Packaging | 1 BOTTLE, DROPPER in 1 CARTON (24208-486-10) / 10 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA090037 |
FDA SPL set id | 744119 |
Labeler | Bausch & Lomb Incorporated |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2009-07-14 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 24208-486 |
NDC Item 42571014726
NDC 9 | 42571-147 |
---|---|
NDC 10 | 42571-147-26 |
NDC Item | 42571014726 |
Packaging | 1 BOTTLE in 1 CARTON (42571-147-26) / 10 mL in 1 BOTTLE |
ANDA | ANDA204777 |
COLORTEXT | white(colorless to nearly colorless) |
Color | C48325 __ |
FDA SPL set id | 812624 |
Labeler | Micro Labs Limited |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2020-06-15 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 42571-147 |
NDC Item 46708055310
NDC 9 | 46708-553 |
---|---|
NDC 10 | 46708-553-10 |
NDC Item | 46708055310 |
Packaging | 1 BOTTLE in 1 CARTON (46708-553-10) / 10 mL in 1 BOTTLE |
ANDA | ANDA213099 |
FDA SPL set id | 827356 |
Labeler | Alembic Pharmaceuticals Limited |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2021-05-04 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 46708-553 |
NDC Item 50090286700
NDC 9 | 50090-2867 |
---|---|
NDC 10 | 50090-2867-0 |
NDC Item | 50090286700 |
Packaging | 1 BOTTLE, DISPENSING in 1 CARTON (50090-2867-0) / 10 mL in 1 BOTTLE, DISPENSING |
ANDA | ANDA202054 |
FDA SPL set id | 302402 |
Labeler | A-S Medication Solutions LLC |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2015-02-17 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 50090-2867 |
NDC Item 50090637100
NDC 9 | 50090-6371 |
---|---|
NDC 10 | 50090-6371-0 |
NDC Item | 50090637100 |
Packaging | 1 BOTTLE, DROPPER in 1 CARTON (50090-6371-0) / 10 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA090037 |
FDA SPL set id | 826332 |
Labeler | A-S Medication Solutions |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2009-07-14 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 50090-6371 |
NDC Item 50090681400
NDC 9 | 50090-6814 |
---|---|
NDC 10 | 50090-6814-0 |
NDC Item | 50090681400 |
Packaging | 1 BOTTLE in 1 CARTON (50090-6814-0) / 10 mL in 1 BOTTLE |
ANDA | ANDA204777 |
COLORTEXT | white(colorless to nearly colorless) |
Color | C48325 __ |
FDA SPL set id | 746492 |
Labeler | A-S Medication Solutions |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2020-06-15 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 50090-6814 |
NDC Item 50383023310
NDC 9 | 50383-233 |
---|---|
NDC 10 | 50383-233-10 |
NDC Item | 50383023310 |
Packaging | 1 BOTTLE, DROPPER in 1 BOX (50383-233-10) / 10 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA077847 |
FDA SPL set id | 640641 |
Labeler | Akorn Operating Company LLC (dba Akorn) |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2008-10-28 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 50383-233 |
NDC Item 60429011510
NDC 9 | 60429-115 |
---|---|
NDC 10 | 60429-115-10 |
NDC Item | 60429011510 |
Packaging | 1 BOTTLE, DROPPER in 1 BOX (60429-115-10) / 10 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA077847 |
FDA SPL set id | 767171 |
Labeler | Golden State Medical Supply, Inc. |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2008-10-28 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 60429-115 |
NDC Item 61314003001
NDC 9 | 61314-030 |
---|---|
NDC 10 | 61314-030-01 |
NDC Item | 61314003001 |
Packaging | 5 mL in 1 BOTTLE (61314-030-01) |
ANDA | ANDA090604 |
FDA SPL set id | 622450 |
Labeler | Sandoz Inc |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2010-01-02 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 61314-030 |
NDC Item 61314003002
NDC 9 | 61314-030 |
---|---|
NDC 10 | 61314-030-02 |
NDC Item | 61314003002 |
Packaging | 10 mL in 1 BOTTLE (61314-030-02) |
ANDA | ANDA090604 |
FDA SPL set id | 622450 |
Labeler | Sandoz Inc |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2010-01-02 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 61314-030 |
NDC Item 62332055310
NDC 9 | 62332-553 |
---|---|
NDC 10 | 62332-553-10 |
NDC Item | 62332055310 |
Packaging | 1 BOTTLE in 1 CARTON (62332-553-10) / 10 mL in 1 BOTTLE |
ANDA | ANDA213099 |
FDA SPL set id | 827411 |
Labeler | Alembic Pharmaceuticals Inc. |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2021-05-04 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 62332-553 |
NDC Item 65862094601
NDC 9 | 65862-946 |
---|---|
NDC 10 | 65862-946-01 |
NDC Item | 65862094601 |
Packaging | 1 BOTTLE, DROPPER in 1 CARTON (65862-946-01) / 10 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA207629 |
FDA SPL set id | 788118 |
Labeler | Aurobindo Pharma Limited |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2021-05-14 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 65862-946 |
NDC Item 68083049001
NDC 9 | 68083-490 |
---|---|
NDC 10 | 68083-490-01 |
NDC Item | 68083049001 |
Packaging | 1 BOTTLE in 1 CARTON (68083-490-01) / 10 mL in 1 BOTTLE |
ANDA | ANDA215520 |
FDA SPL set id | 786662 |
Labeler | Gland Pharma Limited |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2022-09-19 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 68083-490 |
NDC Item 69315030505
NDC 9 | 69315-305 |
---|---|
NDC 10 | 69315-305-05 |
NDC Item | 69315030505 |
Packaging | 1 BOTTLE, PLASTIC in 1 CARTON (69315-305-05) / 5 mL in 1 BOTTLE, PLASTIC |
ANDA | ANDA205295 |
FDA SPL set id | 787995 |
Labeler | Leading Pharma, LLC |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2017-05-18 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 69315-305 |
NDC Item 69315030510
NDC 9 | 69315-305 |
---|---|
NDC 10 | 69315-305-10 |
NDC Item | 69315030510 |
Packaging | 1 BOTTLE, PLASTIC in 1 CARTON (69315-305-10) / 10 mL in 1 BOTTLE, PLASTIC |
ANDA | ANDA205295 |
FDA SPL set id | 787995 |
Labeler | Leading Pharma, LLC |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2017-05-18 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 69315-305 |
NDC Item 70069005101
NDC 9 | 70069-051 |
---|---|
NDC 10 | 70069-051-01 |
NDC Item | 70069005101 |
Packaging | 1 BOTTLE in 1 CARTON (70069-051-01) / 10 mL in 1 BOTTLE |
ANDA | ANDA207523 |
COLORTEXT | WHITE(A clear, colorless to nearly colorless solution) |
Color | C48325 __ |
FDA SPL set id | 755334 |
Labeler | Somerset Therapeutics, LLC |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2019-06-25 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 70069-051 |
NDC Item 70377008211
NDC 9 | 70377-082 |
---|---|
NDC 10 | 70377-082-11 |
NDC Item | 70377008211 |
Packaging | 1 BOTTLE, DISPENSING in 1 CARTON (70377-082-11) / 10 mL in 1 BOTTLE, DISPENSING |
ANDA | ANDA202054 |
FDA SPL set id | 611443 |
Labeler | Biocon Pharma Inc. |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2022-01-08 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 70377-082 |
NDC Item 71921022610
NDC 9 | 71921-226 |
---|---|
NDC 10 | 71921-226-10 |
NDC Item | 71921022610 |
Packaging | 1 BOTTLE, DISPENSING in 1 CARTON (71921-226-10) / 10 mL in 1 BOTTLE, DISPENSING |
ANDA | ANDA202054 |
FDA SPL set id | 724181 |
Labeler | Florida Pharmaceutical Products, LLC |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2023-08-16 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 71921-226 |
NDC Item 72162216602
NDC 9 | 72162-2166 |
---|---|
NDC 10 | 72162-2166-2 |
NDC Item | 72162216602 |
Packaging | 1 BOTTLE, DROPPER in 1 CARTON (72162-2166-2) / 10 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA090037 |
FDA SPL set id | 752883 |
Labeler | Bryant Ranch Prepack |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2009-07-14 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 72162-2166 |
NDC Item 72162218402
NDC 9 | 72162-2184 |
---|---|
NDC 10 | 72162-2184-2 |
NDC Item | 72162218402 |
Packaging | 10 mL in 1 BOTTLE (72162-2184-2) |
ANDA | ANDA090604 |
FDA SPL set id | 753279 |
Labeler | Bryant Ranch Prepack |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2010-01-02 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 72162-2184 |
NDC Item 72162238102
NDC 9 | 72162-2381 |
---|---|
NDC 10 | 72162-2381-2 |
NDC Item | 72162238102 |
Packaging | 1 BOTTLE in 1 CARTON (72162-2381-2) / 10 mL in 1 BOTTLE |
ANDA | ANDA204777 |
COLORTEXT | white(colorless to nearly colorless) |
Color | C48325 __ |
FDA SPL set id | 815591 |
Labeler | Bryant Ranch Prepack |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2020-06-15 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 72162-2381 |
NDC Item 00527176373
NDC 9 | 0527-1763 |
---|---|
NDC 10 | 0527-1763-73 |
NDC Item | 00527176373 |
Packaging | 1 BOTTLE, DROPPER in 1 CARTON (0527-1763-73) / 10 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA201998 |
FDA SPL set id | 447745 |
Labeler | Lannett Company, Inc. |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2014-12-17 |
Marketing status | COMPLETED |
Related queries | Properties for NDC 9 0527-1763 |
NDC Item 00781605470
NDC 9 | 0781-6054 |
---|---|
NDC 10 | 0781-6054-70 |
NDC Item | 00781605470 |
Packaging | 1 BOTTLE, DROPPER in 1 CARTON (0781-6054-70) / 10 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA077847 |
Labeler | Sandoz Inc |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing status | COMPLETED |
Related queries | Properties for NDC 9 0781-6054 |
NDC Item 14445040510
NDC 9 | 14445-405 |
---|---|
NDC 10 | 14445-405-10 |
NDC Item | 14445040510 |
Packaging | 1 BOTTLE, DISPENSING in 1 CARTON (14445-405-10) / 10 mL in 1 BOTTLE, DISPENSING |
ANDA | ANDA202054 |
FDA SPL set id | 837670 |
Labeler | Indoco Remedies Limited |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2021-05-14 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 14445-405 |
NDC Item 24208048605
NDC 9 | 24208-486 |
---|---|
NDC 10 | 24208-486-05 |
NDC Item | 24208048605 |
Packaging | 1 BOTTLE, DROPPER in 1 CARTON (24208-486-05) / 5 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA090037 |
FDA SPL set id | 744119 |
Labeler | Bausch & Lomb Incorporated |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2009-07-14 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 24208-486 |
NDC Item 24208048610
NDC 9 | 24208-486 |
---|---|
NDC 10 | 24208-486-10 |
NDC Item | 24208048610 |
Packaging | 1 BOTTLE, DROPPER in 1 CARTON (24208-486-10) / 10 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA090037 |
FDA SPL set id | 744119 |
Labeler | Bausch & Lomb Incorporated |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2009-07-14 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 24208-486 |
NDC Item 42571014726
NDC 9 | 42571-147 |
---|---|
NDC 10 | 42571-147-26 |
NDC Item | 42571014726 |
Packaging | 1 BOTTLE in 1 CARTON (42571-147-26) / 10 mL in 1 BOTTLE |
ANDA | ANDA204777 |
COLORTEXT | white(colorless to nearly colorless) |
Color | C48325 __ |
FDA SPL set id | 812624 |
Labeler | Micro Labs Limited |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2020-06-15 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 42571-147 |
NDC Item 46708055310
NDC 9 | 46708-553 |
---|---|
NDC 10 | 46708-553-10 |
NDC Item | 46708055310 |
Packaging | 1 BOTTLE in 1 CARTON (46708-553-10) / 10 mL in 1 BOTTLE |
ANDA | ANDA213099 |
FDA SPL set id | 827356 |
Labeler | Alembic Pharmaceuticals Limited |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2021-05-04 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 46708-553 |
NDC Item 50090286700
NDC 9 | 50090-2867 |
---|---|
NDC 10 | 50090-2867-0 |
NDC Item | 50090286700 |
Packaging | 1 BOTTLE, DISPENSING in 1 CARTON (50090-2867-0) / 10 mL in 1 BOTTLE, DISPENSING |
ANDA | ANDA202054 |
FDA SPL set id | 302402 |
Labeler | A-S Medication Solutions LLC |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2015-02-17 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 50090-2867 |
NDC Item 50090637100
NDC 9 | 50090-6371 |
---|---|
NDC 10 | 50090-6371-0 |
NDC Item | 50090637100 |
Packaging | 1 BOTTLE, DROPPER in 1 CARTON (50090-6371-0) / 10 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA090037 |
FDA SPL set id | 826332 |
Labeler | A-S Medication Solutions |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2009-07-14 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 50090-6371 |
NDC Item 50090681400
NDC 9 | 50090-6814 |
---|---|
NDC 10 | 50090-6814-0 |
NDC Item | 50090681400 |
Packaging | 1 BOTTLE in 1 CARTON (50090-6814-0) / 10 mL in 1 BOTTLE |
ANDA | ANDA204777 |
COLORTEXT | white(colorless to nearly colorless) |
Color | C48325 __ |
FDA SPL set id | 746492 |
Labeler | A-S Medication Solutions |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2020-06-15 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 50090-6814 |
NDC Item 50383023310
NDC 9 | 50383-233 |
---|---|
NDC 10 | 50383-233-10 |
NDC Item | 50383023310 |
Packaging | 1 BOTTLE, DROPPER in 1 BOX (50383-233-10) / 10 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA077847 |
FDA SPL set id | 640641 |
Labeler | Akorn Operating Company LLC (dba Akorn) |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2008-10-28 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 50383-233 |
NDC Item 60429011510
NDC 9 | 60429-115 |
---|---|
NDC 10 | 60429-115-10 |
NDC Item | 60429011510 |
Packaging | 1 BOTTLE, DROPPER in 1 BOX (60429-115-10) / 10 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA077847 |
FDA SPL set id | 767171 |
Labeler | Golden State Medical Supply, Inc. |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2008-10-28 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 60429-115 |
NDC Item 61314003001
NDC 9 | 61314-030 |
---|---|
NDC 10 | 61314-030-01 |
NDC Item | 61314003001 |
Packaging | 5 mL in 1 BOTTLE (61314-030-01) |
ANDA | ANDA090604 |
FDA SPL set id | 622450 |
Labeler | Sandoz Inc |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2010-01-02 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 61314-030 |
NDC Item 61314003002
NDC 9 | 61314-030 |
---|---|
NDC 10 | 61314-030-02 |
NDC Item | 61314003002 |
Packaging | 10 mL in 1 BOTTLE (61314-030-02) |
ANDA | ANDA090604 |
FDA SPL set id | 622450 |
Labeler | Sandoz Inc |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2010-01-02 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 61314-030 |
NDC Item 62332055310
NDC 9 | 62332-553 |
---|---|
NDC 10 | 62332-553-10 |
NDC Item | 62332055310 |
Packaging | 1 BOTTLE in 1 CARTON (62332-553-10) / 10 mL in 1 BOTTLE |
ANDA | ANDA213099 |
FDA SPL set id | 827411 |
Labeler | Alembic Pharmaceuticals Inc. |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2021-05-04 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 62332-553 |
NDC Item 65862094601
NDC 9 | 65862-946 |
---|---|
NDC 10 | 65862-946-01 |
NDC Item | 65862094601 |
Packaging | 1 BOTTLE, DROPPER in 1 CARTON (65862-946-01) / 10 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA207629 |
FDA SPL set id | 788118 |
Labeler | Aurobindo Pharma Limited |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2021-05-14 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 65862-946 |
NDC Item 68083049001
NDC 9 | 68083-490 |
---|---|
NDC 10 | 68083-490-01 |
NDC Item | 68083049001 |
Packaging | 1 BOTTLE in 1 CARTON (68083-490-01) / 10 mL in 1 BOTTLE |
ANDA | ANDA215520 |
FDA SPL set id | 786662 |
Labeler | Gland Pharma Limited |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2022-09-19 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 68083-490 |
NDC Item 69315030505
NDC 9 | 69315-305 |
---|---|
NDC 10 | 69315-305-05 |
NDC Item | 69315030505 |
Packaging | 1 BOTTLE, PLASTIC in 1 CARTON (69315-305-05) / 5 mL in 1 BOTTLE, PLASTIC |
ANDA | ANDA205295 |
FDA SPL set id | 787995 |
Labeler | Leading Pharma, LLC |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2017-05-18 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 69315-305 |
NDC Item 69315030510
NDC 9 | 69315-305 |
---|---|
NDC 10 | 69315-305-10 |
NDC Item | 69315030510 |
Packaging | 1 BOTTLE, PLASTIC in 1 CARTON (69315-305-10) / 10 mL in 1 BOTTLE, PLASTIC |
ANDA | ANDA205295 |
FDA SPL set id | 787995 |
Labeler | Leading Pharma, LLC |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2017-05-18 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 69315-305 |
NDC Item 70069005101
NDC 9 | 70069-051 |
---|---|
NDC 10 | 70069-051-01 |
NDC Item | 70069005101 |
Packaging | 1 BOTTLE in 1 CARTON (70069-051-01) / 10 mL in 1 BOTTLE |
ANDA | ANDA207523 |
COLORTEXT | WHITE(A clear, colorless to nearly colorless solution) |
Color | C48325 __ |
FDA SPL set id | 755334 |
Labeler | Somerset Therapeutics, LLC |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2019-06-25 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 70069-051 |
NDC Item 70377008211
NDC 9 | 70377-082 |
---|---|
NDC 10 | 70377-082-11 |
NDC Item | 70377008211 |
Packaging | 1 BOTTLE, DISPENSING in 1 CARTON (70377-082-11) / 10 mL in 1 BOTTLE, DISPENSING |
ANDA | ANDA202054 |
FDA SPL set id | 611443 |
Labeler | Biocon Pharma Inc. |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2022-01-08 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 70377-082 |
NDC Item 71921022610
NDC 9 | 71921-226 |
---|---|
NDC 10 | 71921-226-10 |
NDC Item | 71921022610 |
Packaging | 1 BOTTLE, DISPENSING in 1 CARTON (71921-226-10) / 10 mL in 1 BOTTLE, DISPENSING |
ANDA | ANDA202054 |
FDA SPL set id | 724181 |
Labeler | Florida Pharmaceutical Products, LLC |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2023-08-16 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 71921-226 |
NDC Item 72162216602
NDC 9 | 72162-2166 |
---|---|
NDC 10 | 72162-2166-2 |
NDC Item | 72162216602 |
Packaging | 1 BOTTLE, DROPPER in 1 CARTON (72162-2166-2) / 10 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA090037 |
FDA SPL set id | 752883 |
Labeler | Bryant Ranch Prepack |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2009-07-14 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 72162-2166 |
NDC Item 72162218402
NDC 9 | 72162-2184 |
---|---|
NDC 10 | 72162-2184-2 |
NDC Item | 72162218402 |
Packaging | 10 mL in 1 BOTTLE (72162-2184-2) |
ANDA | ANDA090604 |
FDA SPL set id | 753279 |
Labeler | Bryant Ranch Prepack |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2010-01-02 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 72162-2184 |
NDC Item 72162238102
NDC 9 | 72162-2381 |
---|---|
NDC 10 | 72162-2381-2 |
NDC Item | 72162238102 |
Packaging | 1 BOTTLE in 1 CARTON (72162-2381-2) / 10 mL in 1 BOTTLE |
ANDA | ANDA204777 |
COLORTEXT | white(colorless to nearly colorless) |
Color | C48325 __ |
FDA SPL set id | 815591 |
Labeler | Bryant Ranch Prepack |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2020-06-15 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 72162-2381 |
NDC Item 00527176373
NDC 9 | 0527-1763 |
---|---|
NDC 10 | 0527-1763-73 |
NDC Item | 00527176373 |
Packaging | 1 BOTTLE, DROPPER in 1 CARTON (0527-1763-73) / 10 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA201998 |
FDA SPL set id | 447745 |
Labeler | Lannett Company, Inc. |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2014-12-17 |
Marketing status | COMPLETED |
Related queries | Properties for NDC 9 0527-1763 |
NDC Item 00781605470
NDC 9 | 0781-6054 |
---|---|
NDC 10 | 0781-6054-70 |
NDC Item | 00781605470 |
Packaging | 1 BOTTLE, DROPPER in 1 CARTON (0781-6054-70) / 10 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA077847 |
Labeler | Sandoz Inc |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing status | COMPLETED |
Related queries | Properties for NDC 9 0781-6054 |
NDC Item 14445040510
NDC 9 | 14445-405 |
---|---|
NDC 10 | 14445-405-10 |
NDC Item | 14445040510 |
Packaging | 1 BOTTLE, DISPENSING in 1 CARTON (14445-405-10) / 10 mL in 1 BOTTLE, DISPENSING |
ANDA | ANDA202054 |
FDA SPL set id | 837670 |
Labeler | Indoco Remedies Limited |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2021-05-14 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 14445-405 |
NDC Item 24208048605
NDC 9 | 24208-486 |
---|---|
NDC 10 | 24208-486-05 |
NDC Item | 24208048605 |
Packaging | 1 BOTTLE, DROPPER in 1 CARTON (24208-486-05) / 5 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA090037 |
FDA SPL set id | 744119 |
Labeler | Bausch & Lomb Incorporated |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2009-07-14 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 24208-486 |
NDC Item 24208048610
NDC 9 | 24208-486 |
---|---|
NDC 10 | 24208-486-10 |
NDC Item | 24208048610 |
Packaging | 1 BOTTLE, DROPPER in 1 CARTON (24208-486-10) / 10 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA090037 |
FDA SPL set id | 744119 |
Labeler | Bausch & Lomb Incorporated |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2009-07-14 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 24208-486 |
NDC Item 42571014726
NDC 9 | 42571-147 |
---|---|
NDC 10 | 42571-147-26 |
NDC Item | 42571014726 |
Packaging | 1 BOTTLE in 1 CARTON (42571-147-26) / 10 mL in 1 BOTTLE |
ANDA | ANDA204777 |
COLORTEXT | white(colorless to nearly colorless) |
Color | C48325 __ |
FDA SPL set id | 812624 |
Labeler | Micro Labs Limited |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2020-06-15 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 42571-147 |
NDC Item 46708055310
NDC 9 | 46708-553 |
---|---|
NDC 10 | 46708-553-10 |
NDC Item | 46708055310 |
Packaging | 1 BOTTLE in 1 CARTON (46708-553-10) / 10 mL in 1 BOTTLE |
ANDA | ANDA213099 |
FDA SPL set id | 827356 |
Labeler | Alembic Pharmaceuticals Limited |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2021-05-04 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 46708-553 |
NDC Item 50090286700
NDC 9 | 50090-2867 |
---|---|
NDC 10 | 50090-2867-0 |
NDC Item | 50090286700 |
Packaging | 1 BOTTLE, DISPENSING in 1 CARTON (50090-2867-0) / 10 mL in 1 BOTTLE, DISPENSING |
ANDA | ANDA202054 |
FDA SPL set id | 302402 |
Labeler | A-S Medication Solutions LLC |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2015-02-17 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 50090-2867 |
NDC Item 50090637100
NDC 9 | 50090-6371 |
---|---|
NDC 10 | 50090-6371-0 |
NDC Item | 50090637100 |
Packaging | 1 BOTTLE, DROPPER in 1 CARTON (50090-6371-0) / 10 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA090037 |
FDA SPL set id | 826332 |
Labeler | A-S Medication Solutions |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2009-07-14 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 50090-6371 |
NDC Item 50090681400
NDC 9 | 50090-6814 |
---|---|
NDC 10 | 50090-6814-0 |
NDC Item | 50090681400 |
Packaging | 1 BOTTLE in 1 CARTON (50090-6814-0) / 10 mL in 1 BOTTLE |
ANDA | ANDA204777 |
COLORTEXT | white(colorless to nearly colorless) |
Color | C48325 __ |
FDA SPL set id | 746492 |
Labeler | A-S Medication Solutions |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2020-06-15 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 50090-6814 |
NDC Item 50383023310
NDC 9 | 50383-233 |
---|---|
NDC 10 | 50383-233-10 |
NDC Item | 50383023310 |
Packaging | 1 BOTTLE, DROPPER in 1 BOX (50383-233-10) / 10 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA077847 |
FDA SPL set id | 640641 |
Labeler | Akorn Operating Company LLC (dba Akorn) |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2008-10-28 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 50383-233 |
NDC Item 60429011510
NDC 9 | 60429-115 |
---|---|
NDC 10 | 60429-115-10 |
NDC Item | 60429011510 |
Packaging | 1 BOTTLE, DROPPER in 1 BOX (60429-115-10) / 10 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA077847 |
FDA SPL set id | 767171 |
Labeler | Golden State Medical Supply, Inc. |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2008-10-28 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 60429-115 |
NDC Item 61314003001
NDC 9 | 61314-030 |
---|---|
NDC 10 | 61314-030-01 |
NDC Item | 61314003001 |
Packaging | 5 mL in 1 BOTTLE (61314-030-01) |
ANDA | ANDA090604 |
FDA SPL set id | 622450 |
Labeler | Sandoz Inc |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2010-01-02 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 61314-030 |
NDC Item 61314003002
NDC 9 | 61314-030 |
---|---|
NDC 10 | 61314-030-02 |
NDC Item | 61314003002 |
Packaging | 10 mL in 1 BOTTLE (61314-030-02) |
ANDA | ANDA090604 |
FDA SPL set id | 622450 |
Labeler | Sandoz Inc |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2010-01-02 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 61314-030 |
NDC Item 62332055310
NDC 9 | 62332-553 |
---|---|
NDC 10 | 62332-553-10 |
NDC Item | 62332055310 |
Packaging | 1 BOTTLE in 1 CARTON (62332-553-10) / 10 mL in 1 BOTTLE |
ANDA | ANDA213099 |
FDA SPL set id | 827411 |
Labeler | Alembic Pharmaceuticals Inc. |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2021-05-04 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 62332-553 |
NDC Item 65862094601
NDC 9 | 65862-946 |
---|---|
NDC 10 | 65862-946-01 |
NDC Item | 65862094601 |
Packaging | 1 BOTTLE, DROPPER in 1 CARTON (65862-946-01) / 10 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA207629 |
FDA SPL set id | 788118 |
Labeler | Aurobindo Pharma Limited |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2021-05-14 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 65862-946 |
NDC Item 68083049001
NDC 9 | 68083-490 |
---|---|
NDC 10 | 68083-490-01 |
NDC Item | 68083049001 |
Packaging | 1 BOTTLE in 1 CARTON (68083-490-01) / 10 mL in 1 BOTTLE |
ANDA | ANDA215520 |
FDA SPL set id | 786662 |
Labeler | Gland Pharma Limited |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2022-09-19 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 68083-490 |
NDC Item 69315030505
NDC 9 | 69315-305 |
---|---|
NDC 10 | 69315-305-05 |
NDC Item | 69315030505 |
Packaging | 1 BOTTLE, PLASTIC in 1 CARTON (69315-305-05) / 5 mL in 1 BOTTLE, PLASTIC |
ANDA | ANDA205295 |
FDA SPL set id | 787995 |
Labeler | Leading Pharma, LLC |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2017-05-18 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 69315-305 |
NDC Item 69315030510
NDC 9 | 69315-305 |
---|---|
NDC 10 | 69315-305-10 |
NDC Item | 69315030510 |
Packaging | 1 BOTTLE, PLASTIC in 1 CARTON (69315-305-10) / 10 mL in 1 BOTTLE, PLASTIC |
ANDA | ANDA205295 |
FDA SPL set id | 787995 |
Labeler | Leading Pharma, LLC |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2017-05-18 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 69315-305 |
NDC Item 70069005101
NDC 9 | 70069-051 |
---|---|
NDC 10 | 70069-051-01 |
NDC Item | 70069005101 |
Packaging | 1 BOTTLE in 1 CARTON (70069-051-01) / 10 mL in 1 BOTTLE |
ANDA | ANDA207523 |
COLORTEXT | WHITE(A clear, colorless to nearly colorless solution) |
Color | C48325 __ |
FDA SPL set id | 755334 |
Labeler | Somerset Therapeutics, LLC |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2019-06-25 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 70069-051 |
NDC Item 70377008211
NDC 9 | 70377-082 |
---|---|
NDC 10 | 70377-082-11 |
NDC Item | 70377008211 |
Packaging | 1 BOTTLE, DISPENSING in 1 CARTON (70377-082-11) / 10 mL in 1 BOTTLE, DISPENSING |
ANDA | ANDA202054 |
FDA SPL set id | 611443 |
Labeler | Biocon Pharma Inc. |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2022-01-08 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 70377-082 |
NDC Item 71921022610
NDC 9 | 71921-226 |
---|---|
NDC 10 | 71921-226-10 |
NDC Item | 71921022610 |
Packaging | 1 BOTTLE, DISPENSING in 1 CARTON (71921-226-10) / 10 mL in 1 BOTTLE, DISPENSING |
ANDA | ANDA202054 |
FDA SPL set id | 724181 |
Labeler | Florida Pharmaceutical Products, LLC |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2023-08-16 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 71921-226 |
NDC Item 72162216602
NDC 9 | 72162-2166 |
---|---|
NDC 10 | 72162-2166-2 |
NDC Item | 72162216602 |
Packaging | 1 BOTTLE, DROPPER in 1 CARTON (72162-2166-2) / 10 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA090037 |
FDA SPL set id | 752883 |
Labeler | Bryant Ranch Prepack |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2009-07-14 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 72162-2166 |
NDC Item 72162218402
NDC 9 | 72162-2184 |
---|---|
NDC 10 | 72162-2184-2 |
NDC Item | 72162218402 |
Packaging | 10 mL in 1 BOTTLE (72162-2184-2) |
ANDA | ANDA090604 |
FDA SPL set id | 753279 |
Labeler | Bryant Ranch Prepack |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2010-01-02 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 72162-2184 |
NDC Item 72162238102
NDC 9 | 72162-2381 |
---|---|
NDC 10 | 72162-2381-2 |
NDC Item | 72162238102 |
Packaging | 1 BOTTLE in 1 CARTON (72162-2381-2) / 10 mL in 1 BOTTLE |
ANDA | ANDA204777 |
COLORTEXT | white(colorless to nearly colorless) |
Color | C48325 __ |
FDA SPL set id | 815591 |
Labeler | Bryant Ranch Prepack |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2020-06-15 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 72162-2381 |
NDC Item 00527176373
NDC 9 | 0527-1763 |
---|---|
NDC 10 | 0527-1763-73 |
NDC Item | 00527176373 |
Packaging | 1 BOTTLE, DROPPER in 1 CARTON (0527-1763-73) / 10 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA201998 |
FDA SPL set id | 447745 |
Labeler | Lannett Company, Inc. |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2014-12-17 |
Marketing status | COMPLETED |
Related queries | Properties for NDC 9 0527-1763 |
NDC Item 00781605470
NDC 9 | 0781-6054 |
---|---|
NDC 10 | 0781-6054-70 |
NDC Item | 00781605470 |
Packaging | 1 BOTTLE, DROPPER in 1 CARTON (0781-6054-70) / 10 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA077847 |
Labeler | Sandoz Inc |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing status | COMPLETED |
Related queries | Properties for NDC 9 0781-6054 |
NDC Item 14445040510
NDC 9 | 14445-405 |
---|---|
NDC 10 | 14445-405-10 |
NDC Item | 14445040510 |
Packaging | 1 BOTTLE, DISPENSING in 1 CARTON (14445-405-10) / 10 mL in 1 BOTTLE, DISPENSING |
ANDA | ANDA202054 |
FDA SPL set id | 837670 |
Labeler | Indoco Remedies Limited |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2021-05-14 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 14445-405 |
NDC Item 24208048605
NDC 9 | 24208-486 |
---|---|
NDC 10 | 24208-486-05 |
NDC Item | 24208048605 |
Packaging | 1 BOTTLE, DROPPER in 1 CARTON (24208-486-05) / 5 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA090037 |
FDA SPL set id | 744119 |
Labeler | Bausch & Lomb Incorporated |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2009-07-14 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 24208-486 |
NDC Item 24208048610
NDC 9 | 24208-486 |
---|---|
NDC 10 | 24208-486-10 |
NDC Item | 24208048610 |
Packaging | 1 BOTTLE, DROPPER in 1 CARTON (24208-486-10) / 10 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA090037 |
FDA SPL set id | 744119 |
Labeler | Bausch & Lomb Incorporated |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2009-07-14 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 24208-486 |
NDC Item 42571014726
NDC 9 | 42571-147 |
---|---|
NDC 10 | 42571-147-26 |
NDC Item | 42571014726 |
Packaging | 1 BOTTLE in 1 CARTON (42571-147-26) / 10 mL in 1 BOTTLE |
ANDA | ANDA204777 |
COLORTEXT | white(colorless to nearly colorless) |
Color | C48325 __ |
FDA SPL set id | 812624 |
Labeler | Micro Labs Limited |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2020-06-15 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 42571-147 |
NDC Item 46708055310
NDC 9 | 46708-553 |
---|---|
NDC 10 | 46708-553-10 |
NDC Item | 46708055310 |
Packaging | 1 BOTTLE in 1 CARTON (46708-553-10) / 10 mL in 1 BOTTLE |
ANDA | ANDA213099 |
FDA SPL set id | 827356 |
Labeler | Alembic Pharmaceuticals Limited |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2021-05-04 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 46708-553 |
NDC Item 50090286700
NDC 9 | 50090-2867 |
---|---|
NDC 10 | 50090-2867-0 |
NDC Item | 50090286700 |
Packaging | 1 BOTTLE, DISPENSING in 1 CARTON (50090-2867-0) / 10 mL in 1 BOTTLE, DISPENSING |
ANDA | ANDA202054 |
FDA SPL set id | 302402 |
Labeler | A-S Medication Solutions LLC |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2015-02-17 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 50090-2867 |
NDC Item 50090637100
NDC 9 | 50090-6371 |
---|---|
NDC 10 | 50090-6371-0 |
NDC Item | 50090637100 |
Packaging | 1 BOTTLE, DROPPER in 1 CARTON (50090-6371-0) / 10 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA090037 |
FDA SPL set id | 826332 |
Labeler | A-S Medication Solutions |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2009-07-14 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 50090-6371 |
NDC Item 50090681400
NDC 9 | 50090-6814 |
---|---|
NDC 10 | 50090-6814-0 |
NDC Item | 50090681400 |
Packaging | 1 BOTTLE in 1 CARTON (50090-6814-0) / 10 mL in 1 BOTTLE |
ANDA | ANDA204777 |
COLORTEXT | white(colorless to nearly colorless) |
Color | C48325 __ |
FDA SPL set id | 746492 |
Labeler | A-S Medication Solutions |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2020-06-15 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 50090-6814 |
NDC Item 50383023310
NDC 9 | 50383-233 |
---|---|
NDC 10 | 50383-233-10 |
NDC Item | 50383023310 |
Packaging | 1 BOTTLE, DROPPER in 1 BOX (50383-233-10) / 10 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA077847 |
FDA SPL set id | 640641 |
Labeler | Akorn Operating Company LLC (dba Akorn) |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2008-10-28 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 50383-233 |
NDC Item 60429011510
NDC 9 | 60429-115 |
---|---|
NDC 10 | 60429-115-10 |
NDC Item | 60429011510 |
Packaging | 1 BOTTLE, DROPPER in 1 BOX (60429-115-10) / 10 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA077847 |
FDA SPL set id | 767171 |
Labeler | Golden State Medical Supply, Inc. |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2008-10-28 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 60429-115 |
NDC Item 61314003001
NDC 9 | 61314-030 |
---|---|
NDC 10 | 61314-030-01 |
NDC Item | 61314003001 |
Packaging | 5 mL in 1 BOTTLE (61314-030-01) |
ANDA | ANDA090604 |
FDA SPL set id | 622450 |
Labeler | Sandoz Inc |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2010-01-02 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 61314-030 |
NDC Item 61314003002
NDC 9 | 61314-030 |
---|---|
NDC 10 | 61314-030-02 |
NDC Item | 61314003002 |
Packaging | 10 mL in 1 BOTTLE (61314-030-02) |
ANDA | ANDA090604 |
FDA SPL set id | 622450 |
Labeler | Sandoz Inc |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2010-01-02 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 61314-030 |
NDC Item 62332055310
NDC 9 | 62332-553 |
---|---|
NDC 10 | 62332-553-10 |
NDC Item | 62332055310 |
Packaging | 1 BOTTLE in 1 CARTON (62332-553-10) / 10 mL in 1 BOTTLE |
ANDA | ANDA213099 |
FDA SPL set id | 827411 |
Labeler | Alembic Pharmaceuticals Inc. |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2021-05-04 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 62332-553 |
NDC Item 65862094601
NDC 9 | 65862-946 |
---|---|
NDC 10 | 65862-946-01 |
NDC Item | 65862094601 |
Packaging | 1 BOTTLE, DROPPER in 1 CARTON (65862-946-01) / 10 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA207629 |
FDA SPL set id | 788118 |
Labeler | Aurobindo Pharma Limited |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2021-05-14 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 65862-946 |
NDC Item 68083049001
NDC 9 | 68083-490 |
---|---|
NDC 10 | 68083-490-01 |
NDC Item | 68083049001 |
Packaging | 1 BOTTLE in 1 CARTON (68083-490-01) / 10 mL in 1 BOTTLE |
ANDA | ANDA215520 |
FDA SPL set id | 786662 |
Labeler | Gland Pharma Limited |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2022-09-19 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 68083-490 |
NDC Item 69315030505
NDC 9 | 69315-305 |
---|---|
NDC 10 | 69315-305-05 |
NDC Item | 69315030505 |
Packaging | 1 BOTTLE, PLASTIC in 1 CARTON (69315-305-05) / 5 mL in 1 BOTTLE, PLASTIC |
ANDA | ANDA205295 |
FDA SPL set id | 787995 |
Labeler | Leading Pharma, LLC |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2017-05-18 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 69315-305 |
NDC Item 69315030510
NDC 9 | 69315-305 |
---|---|
NDC 10 | 69315-305-10 |
NDC Item | 69315030510 |
Packaging | 1 BOTTLE, PLASTIC in 1 CARTON (69315-305-10) / 10 mL in 1 BOTTLE, PLASTIC |
ANDA | ANDA205295 |
FDA SPL set id | 787995 |
Labeler | Leading Pharma, LLC |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2017-05-18 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 69315-305 |
NDC Item 70069005101
NDC 9 | 70069-051 |
---|---|
NDC 10 | 70069-051-01 |
NDC Item | 70069005101 |
Packaging | 1 BOTTLE in 1 CARTON (70069-051-01) / 10 mL in 1 BOTTLE |
ANDA | ANDA207523 |
COLORTEXT | WHITE(A clear, colorless to nearly colorless solution) |
Color | C48325 __ |
FDA SPL set id | 755334 |
Labeler | Somerset Therapeutics, LLC |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2019-06-25 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 70069-051 |
NDC Item 70377008211
NDC 9 | 70377-082 |
---|---|
NDC 10 | 70377-082-11 |
NDC Item | 70377008211 |
Packaging | 1 BOTTLE, DISPENSING in 1 CARTON (70377-082-11) / 10 mL in 1 BOTTLE, DISPENSING |
ANDA | ANDA202054 |
FDA SPL set id | 611443 |
Labeler | Biocon Pharma Inc. |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2022-01-08 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 70377-082 |
NDC Item 71921022610
NDC 9 | 71921-226 |
---|---|
NDC 10 | 71921-226-10 |
NDC Item | 71921022610 |
Packaging | 1 BOTTLE, DISPENSING in 1 CARTON (71921-226-10) / 10 mL in 1 BOTTLE, DISPENSING |
ANDA | ANDA202054 |
FDA SPL set id | 724181 |
Labeler | Florida Pharmaceutical Products, LLC |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2023-08-16 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 71921-226 |
NDC Item 72162216602
NDC 9 | 72162-2166 |
---|---|
NDC 10 | 72162-2166-2 |
NDC Item | 72162216602 |
Packaging | 1 BOTTLE, DROPPER in 1 CARTON (72162-2166-2) / 10 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA090037 |
FDA SPL set id | 752883 |
Labeler | Bryant Ranch Prepack |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2009-07-14 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 72162-2166 |
NDC Item 72162218402
NDC 9 | 72162-2184 |
---|---|
NDC 10 | 72162-2184-2 |
NDC Item | 72162218402 |
Packaging | 10 mL in 1 BOTTLE (72162-2184-2) |
ANDA | ANDA090604 |
FDA SPL set id | 753279 |
Labeler | Bryant Ranch Prepack |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2010-01-02 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 72162-2184 |
NDC Item 72162238102
NDC 9 | 72162-2381 |
---|---|
NDC 10 | 72162-2381-2 |
NDC Item | 72162238102 |
Packaging | 1 BOTTLE in 1 CARTON (72162-2381-2) / 10 mL in 1 BOTTLE |
ANDA | ANDA204777 |
COLORTEXT | white(colorless to nearly colorless) |
Color | C48325 __ |
FDA SPL set id | 815591 |
Labeler | Bryant Ranch Prepack |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2020-06-15 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 72162-2381 |
NDC Item 00527176373
NDC 9 | 0527-1763 |
---|---|
NDC 10 | 0527-1763-73 |
NDC Item | 00527176373 |
Packaging | 1 BOTTLE, DROPPER in 1 CARTON (0527-1763-73) / 10 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA201998 |
FDA SPL set id | 447745 |
Labeler | Lannett Company, Inc. |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2014-12-17 |
Marketing status | COMPLETED |
Related queries | Properties for NDC 9 0527-1763 |
NDC Item 00781605470
NDC 9 | 0781-6054 |
---|---|
NDC 10 | 0781-6054-70 |
NDC Item | 00781605470 |
Packaging | 1 BOTTLE, DROPPER in 1 CARTON (0781-6054-70) / 10 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA077847 |
Labeler | Sandoz Inc |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing status | COMPLETED |
Related queries | Properties for NDC 9 0781-6054 |
NDC Item 14445040510
NDC 9 | 14445-405 |
---|---|
NDC 10 | 14445-405-10 |
NDC Item | 14445040510 |
Packaging | 1 BOTTLE, DISPENSING in 1 CARTON (14445-405-10) / 10 mL in 1 BOTTLE, DISPENSING |
ANDA | ANDA202054 |
FDA SPL set id | 837670 |
Labeler | Indoco Remedies Limited |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2021-05-14 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 14445-405 |
NDC Item 24208048605
NDC 9 | 24208-486 |
---|---|
NDC 10 | 24208-486-05 |
NDC Item | 24208048605 |
Packaging | 1 BOTTLE, DROPPER in 1 CARTON (24208-486-05) / 5 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA090037 |
FDA SPL set id | 744119 |
Labeler | Bausch & Lomb Incorporated |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2009-07-14 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 24208-486 |
NDC Item 24208048610
NDC 9 | 24208-486 |
---|---|
NDC 10 | 24208-486-10 |
NDC Item | 24208048610 |
Packaging | 1 BOTTLE, DROPPER in 1 CARTON (24208-486-10) / 10 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA090037 |
FDA SPL set id | 744119 |
Labeler | Bausch & Lomb Incorporated |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2009-07-14 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 24208-486 |
NDC Item 42571014726
NDC 9 | 42571-147 |
---|---|
NDC 10 | 42571-147-26 |
NDC Item | 42571014726 |
Packaging | 1 BOTTLE in 1 CARTON (42571-147-26) / 10 mL in 1 BOTTLE |
ANDA | ANDA204777 |
COLORTEXT | white(colorless to nearly colorless) |
Color | C48325 __ |
FDA SPL set id | 812624 |
Labeler | Micro Labs Limited |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2020-06-15 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 42571-147 |
NDC Item 46708055310
NDC 9 | 46708-553 |
---|---|
NDC 10 | 46708-553-10 |
NDC Item | 46708055310 |
Packaging | 1 BOTTLE in 1 CARTON (46708-553-10) / 10 mL in 1 BOTTLE |
ANDA | ANDA213099 |
FDA SPL set id | 827356 |
Labeler | Alembic Pharmaceuticals Limited |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2021-05-04 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 46708-553 |
NDC Item 50090286700
NDC 9 | 50090-2867 |
---|---|
NDC 10 | 50090-2867-0 |
NDC Item | 50090286700 |
Packaging | 1 BOTTLE, DISPENSING in 1 CARTON (50090-2867-0) / 10 mL in 1 BOTTLE, DISPENSING |
ANDA | ANDA202054 |
FDA SPL set id | 302402 |
Labeler | A-S Medication Solutions LLC |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2015-02-17 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 50090-2867 |
NDC Item 50090637100
NDC 9 | 50090-6371 |
---|---|
NDC 10 | 50090-6371-0 |
NDC Item | 50090637100 |
Packaging | 1 BOTTLE, DROPPER in 1 CARTON (50090-6371-0) / 10 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA090037 |
FDA SPL set id | 826332 |
Labeler | A-S Medication Solutions |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2009-07-14 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 50090-6371 |
NDC Item 50090681400
NDC 9 | 50090-6814 |
---|---|
NDC 10 | 50090-6814-0 |
NDC Item | 50090681400 |
Packaging | 1 BOTTLE in 1 CARTON (50090-6814-0) / 10 mL in 1 BOTTLE |
ANDA | ANDA204777 |
COLORTEXT | white(colorless to nearly colorless) |
Color | C48325 __ |
FDA SPL set id | 746492 |
Labeler | A-S Medication Solutions |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2020-06-15 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 50090-6814 |
NDC Item 50383023310
NDC 9 | 50383-233 |
---|---|
NDC 10 | 50383-233-10 |
NDC Item | 50383023310 |
Packaging | 1 BOTTLE, DROPPER in 1 BOX (50383-233-10) / 10 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA077847 |
FDA SPL set id | 640641 |
Labeler | Akorn Operating Company LLC (dba Akorn) |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2008-10-28 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 50383-233 |
NDC Item 60429011510
NDC 9 | 60429-115 |
---|---|
NDC 10 | 60429-115-10 |
NDC Item | 60429011510 |
Packaging | 1 BOTTLE, DROPPER in 1 BOX (60429-115-10) / 10 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA077847 |
FDA SPL set id | 767171 |
Labeler | Golden State Medical Supply, Inc. |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2008-10-28 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 60429-115 |
NDC Item 61314003001
NDC 9 | 61314-030 |
---|---|
NDC 10 | 61314-030-01 |
NDC Item | 61314003001 |
Packaging | 5 mL in 1 BOTTLE (61314-030-01) |
ANDA | ANDA090604 |
FDA SPL set id | 622450 |
Labeler | Sandoz Inc |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2010-01-02 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 61314-030 |
NDC Item 61314003002
NDC 9 | 61314-030 |
---|---|
NDC 10 | 61314-030-02 |
NDC Item | 61314003002 |
Packaging | 10 mL in 1 BOTTLE (61314-030-02) |
ANDA | ANDA090604 |
FDA SPL set id | 622450 |
Labeler | Sandoz Inc |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2010-01-02 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 61314-030 |
NDC Item 62332055310
NDC 9 | 62332-553 |
---|---|
NDC 10 | 62332-553-10 |
NDC Item | 62332055310 |
Packaging | 1 BOTTLE in 1 CARTON (62332-553-10) / 10 mL in 1 BOTTLE |
ANDA | ANDA213099 |
FDA SPL set id | 827411 |
Labeler | Alembic Pharmaceuticals Inc. |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2021-05-04 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 62332-553 |
NDC Item 65862094601
NDC 9 | 65862-946 |
---|---|
NDC 10 | 65862-946-01 |
NDC Item | 65862094601 |
Packaging | 1 BOTTLE, DROPPER in 1 CARTON (65862-946-01) / 10 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA207629 |
FDA SPL set id | 788118 |
Labeler | Aurobindo Pharma Limited |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2021-05-14 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 65862-946 |
NDC Item 68083049001
NDC 9 | 68083-490 |
---|---|
NDC 10 | 68083-490-01 |
NDC Item | 68083049001 |
Packaging | 1 BOTTLE in 1 CARTON (68083-490-01) / 10 mL in 1 BOTTLE |
ANDA | ANDA215520 |
FDA SPL set id | 786662 |
Labeler | Gland Pharma Limited |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2022-09-19 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 68083-490 |
NDC Item 69315030505
NDC 9 | 69315-305 |
---|---|
NDC 10 | 69315-305-05 |
NDC Item | 69315030505 |
Packaging | 1 BOTTLE, PLASTIC in 1 CARTON (69315-305-05) / 5 mL in 1 BOTTLE, PLASTIC |
ANDA | ANDA205295 |
FDA SPL set id | 787995 |
Labeler | Leading Pharma, LLC |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2017-05-18 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 69315-305 |
NDC Item 69315030510
NDC 9 | 69315-305 |
---|---|
NDC 10 | 69315-305-10 |
NDC Item | 69315030510 |
Packaging | 1 BOTTLE, PLASTIC in 1 CARTON (69315-305-10) / 10 mL in 1 BOTTLE, PLASTIC |
ANDA | ANDA205295 |
FDA SPL set id | 787995 |
Labeler | Leading Pharma, LLC |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2017-05-18 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 69315-305 |
NDC Item 70069005101
NDC 9 | 70069-051 |
---|---|
NDC 10 | 70069-051-01 |
NDC Item | 70069005101 |
Packaging | 1 BOTTLE in 1 CARTON (70069-051-01) / 10 mL in 1 BOTTLE |
ANDA | ANDA207523 |
COLORTEXT | WHITE(A clear, colorless to nearly colorless solution) |
Color | C48325 __ |
FDA SPL set id | 755334 |
Labeler | Somerset Therapeutics, LLC |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2019-06-25 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 70069-051 |
NDC Item 70377008211
NDC 9 | 70377-082 |
---|---|
NDC 10 | 70377-082-11 |
NDC Item | 70377008211 |
Packaging | 1 BOTTLE, DISPENSING in 1 CARTON (70377-082-11) / 10 mL in 1 BOTTLE, DISPENSING |
ANDA | ANDA202054 |
FDA SPL set id | 611443 |
Labeler | Biocon Pharma Inc. |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2022-01-08 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 70377-082 |
NDC Item 71921022610
NDC 9 | 71921-226 |
---|---|
NDC 10 | 71921-226-10 |
NDC Item | 71921022610 |
Packaging | 1 BOTTLE, DISPENSING in 1 CARTON (71921-226-10) / 10 mL in 1 BOTTLE, DISPENSING |
ANDA | ANDA202054 |
FDA SPL set id | 724181 |
Labeler | Florida Pharmaceutical Products, LLC |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2023-08-16 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 71921-226 |
NDC Item 72162216602
NDC 9 | 72162-2166 |
---|---|
NDC 10 | 72162-2166-2 |
NDC Item | 72162216602 |
Packaging | 1 BOTTLE, DROPPER in 1 CARTON (72162-2166-2) / 10 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA090037 |
FDA SPL set id | 752883 |
Labeler | Bryant Ranch Prepack |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2009-07-14 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 72162-2166 |
NDC Item 72162218402
NDC 9 | 72162-2184 |
---|---|
NDC 10 | 72162-2184-2 |
NDC Item | 72162218402 |
Packaging | 10 mL in 1 BOTTLE (72162-2184-2) |
ANDA | ANDA090604 |
FDA SPL set id | 753279 |
Labeler | Bryant Ranch Prepack |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2010-01-02 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 72162-2184 |
NDC Item 72162238102
NDC 9 | 72162-2381 |
---|---|
NDC 10 | 72162-2381-2 |
NDC Item | 72162238102 |
Packaging | 1 BOTTLE in 1 CARTON (72162-2381-2) / 10 mL in 1 BOTTLE |
ANDA | ANDA204777 |
COLORTEXT | white(colorless to nearly colorless) |
Color | C48325 __ |
FDA SPL set id | 815591 |
Labeler | Bryant Ranch Prepack |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2020-06-15 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 72162-2381 |
NDC Item 00527176373
NDC 9 | 0527-1763 |
---|---|
NDC 10 | 0527-1763-73 |
NDC Item | 00527176373 |
Packaging | 1 BOTTLE, DROPPER in 1 CARTON (0527-1763-73) / 10 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA201998 |
FDA SPL set id | 447745 |
Labeler | Lannett Company, Inc. |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2014-12-17 |
Marketing status | COMPLETED |
Related queries | Properties for NDC 9 0527-1763 |
NDC Item 00781605470
NDC 9 | 0781-6054 |
---|---|
NDC 10 | 0781-6054-70 |
NDC Item | 00781605470 |
Packaging | 1 BOTTLE, DROPPER in 1 CARTON (0781-6054-70) / 10 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA077847 |
Labeler | Sandoz Inc |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing status | COMPLETED |
Related queries | Properties for NDC 9 0781-6054 |
NDC Item 14445040510
NDC 9 | 14445-405 |
---|---|
NDC 10 | 14445-405-10 |
NDC Item | 14445040510 |
Packaging | 1 BOTTLE, DISPENSING in 1 CARTON (14445-405-10) / 10 mL in 1 BOTTLE, DISPENSING |
ANDA | ANDA202054 |
FDA SPL set id | 837670 |
Labeler | Indoco Remedies Limited |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2021-05-14 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 14445-405 |
NDC Item 24208048605
NDC 9 | 24208-486 |
---|---|
NDC 10 | 24208-486-05 |
NDC Item | 24208048605 |
Packaging | 1 BOTTLE, DROPPER in 1 CARTON (24208-486-05) / 5 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA090037 |
FDA SPL set id | 744119 |
Labeler | Bausch & Lomb Incorporated |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2009-07-14 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 24208-486 |
NDC Item 24208048610
NDC 9 | 24208-486 |
---|---|
NDC 10 | 24208-486-10 |
NDC Item | 24208048610 |
Packaging | 1 BOTTLE, DROPPER in 1 CARTON (24208-486-10) / 10 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA090037 |
FDA SPL set id | 744119 |
Labeler | Bausch & Lomb Incorporated |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2009-07-14 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 24208-486 |
NDC Item 42571014726
NDC 9 | 42571-147 |
---|---|
NDC 10 | 42571-147-26 |
NDC Item | 42571014726 |
Packaging | 1 BOTTLE in 1 CARTON (42571-147-26) / 10 mL in 1 BOTTLE |
ANDA | ANDA204777 |
COLORTEXT | white(colorless to nearly colorless) |
Color | C48325 __ |
FDA SPL set id | 812624 |
Labeler | Micro Labs Limited |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2020-06-15 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 42571-147 |
NDC Item 46708055310
NDC 9 | 46708-553 |
---|---|
NDC 10 | 46708-553-10 |
NDC Item | 46708055310 |
Packaging | 1 BOTTLE in 1 CARTON (46708-553-10) / 10 mL in 1 BOTTLE |
ANDA | ANDA213099 |
FDA SPL set id | 827356 |
Labeler | Alembic Pharmaceuticals Limited |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2021-05-04 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 46708-553 |
NDC Item 50090286700
NDC 9 | 50090-2867 |
---|---|
NDC 10 | 50090-2867-0 |
NDC Item | 50090286700 |
Packaging | 1 BOTTLE, DISPENSING in 1 CARTON (50090-2867-0) / 10 mL in 1 BOTTLE, DISPENSING |
ANDA | ANDA202054 |
FDA SPL set id | 302402 |
Labeler | A-S Medication Solutions LLC |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2015-02-17 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 50090-2867 |
NDC Item 50090637100
NDC 9 | 50090-6371 |
---|---|
NDC 10 | 50090-6371-0 |
NDC Item | 50090637100 |
Packaging | 1 BOTTLE, DROPPER in 1 CARTON (50090-6371-0) / 10 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA090037 |
FDA SPL set id | 826332 |
Labeler | A-S Medication Solutions |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2009-07-14 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 50090-6371 |
NDC Item 50090681400
NDC 9 | 50090-6814 |
---|---|
NDC 10 | 50090-6814-0 |
NDC Item | 50090681400 |
Packaging | 1 BOTTLE in 1 CARTON (50090-6814-0) / 10 mL in 1 BOTTLE |
ANDA | ANDA204777 |
COLORTEXT | white(colorless to nearly colorless) |
Color | C48325 __ |
FDA SPL set id | 746492 |
Labeler | A-S Medication Solutions |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2020-06-15 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 50090-6814 |
NDC Item 50383023310
NDC 9 | 50383-233 |
---|---|
NDC 10 | 50383-233-10 |
NDC Item | 50383023310 |
Packaging | 1 BOTTLE, DROPPER in 1 BOX (50383-233-10) / 10 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA077847 |
FDA SPL set id | 640641 |
Labeler | Akorn Operating Company LLC (dba Akorn) |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2008-10-28 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 50383-233 |
NDC Item 60429011510
NDC 9 | 60429-115 |
---|---|
NDC 10 | 60429-115-10 |
NDC Item | 60429011510 |
Packaging | 1 BOTTLE, DROPPER in 1 BOX (60429-115-10) / 10 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA077847 |
FDA SPL set id | 767171 |
Labeler | Golden State Medical Supply, Inc. |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2008-10-28 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 60429-115 |
NDC Item 61314003001
NDC 9 | 61314-030 |
---|---|
NDC 10 | 61314-030-01 |
NDC Item | 61314003001 |
Packaging | 5 mL in 1 BOTTLE (61314-030-01) |
ANDA | ANDA090604 |
FDA SPL set id | 622450 |
Labeler | Sandoz Inc |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2010-01-02 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 61314-030 |
NDC Item 61314003002
NDC 9 | 61314-030 |
---|---|
NDC 10 | 61314-030-02 |
NDC Item | 61314003002 |
Packaging | 10 mL in 1 BOTTLE (61314-030-02) |
ANDA | ANDA090604 |
FDA SPL set id | 622450 |
Labeler | Sandoz Inc |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2010-01-02 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 61314-030 |
NDC Item 62332055310
NDC 9 | 62332-553 |
---|---|
NDC 10 | 62332-553-10 |
NDC Item | 62332055310 |
Packaging | 1 BOTTLE in 1 CARTON (62332-553-10) / 10 mL in 1 BOTTLE |
ANDA | ANDA213099 |
FDA SPL set id | 827411 |
Labeler | Alembic Pharmaceuticals Inc. |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2021-05-04 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 62332-553 |
NDC Item 65862094601
NDC 9 | 65862-946 |
---|---|
NDC 10 | 65862-946-01 |
NDC Item | 65862094601 |
Packaging | 1 BOTTLE, DROPPER in 1 CARTON (65862-946-01) / 10 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA207629 |
FDA SPL set id | 788118 |
Labeler | Aurobindo Pharma Limited |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2021-05-14 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 65862-946 |
NDC Item 68083049001
NDC 9 | 68083-490 |
---|---|
NDC 10 | 68083-490-01 |
NDC Item | 68083049001 |
Packaging | 1 BOTTLE in 1 CARTON (68083-490-01) / 10 mL in 1 BOTTLE |
ANDA | ANDA215520 |
FDA SPL set id | 786662 |
Labeler | Gland Pharma Limited |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2022-09-19 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 68083-490 |
NDC Item 69315030505
NDC 9 | 69315-305 |
---|---|
NDC 10 | 69315-305-05 |
NDC Item | 69315030505 |
Packaging | 1 BOTTLE, PLASTIC in 1 CARTON (69315-305-05) / 5 mL in 1 BOTTLE, PLASTIC |
ANDA | ANDA205295 |
FDA SPL set id | 787995 |
Labeler | Leading Pharma, LLC |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2017-05-18 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 69315-305 |
NDC Item 69315030510
NDC 9 | 69315-305 |
---|---|
NDC 10 | 69315-305-10 |
NDC Item | 69315030510 |
Packaging | 1 BOTTLE, PLASTIC in 1 CARTON (69315-305-10) / 10 mL in 1 BOTTLE, PLASTIC |
ANDA | ANDA205295 |
FDA SPL set id | 787995 |
Labeler | Leading Pharma, LLC |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2017-05-18 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 69315-305 |
NDC Item 70069005101
NDC 9 | 70069-051 |
---|---|
NDC 10 | 70069-051-01 |
NDC Item | 70069005101 |
Packaging | 1 BOTTLE in 1 CARTON (70069-051-01) / 10 mL in 1 BOTTLE |
ANDA | ANDA207523 |
COLORTEXT | WHITE(A clear, colorless to nearly colorless solution) |
Color | C48325 __ |
FDA SPL set id | 755334 |
Labeler | Somerset Therapeutics, LLC |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2019-06-25 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 70069-051 |
NDC Item 70377008211
NDC 9 | 70377-082 |
---|---|
NDC 10 | 70377-082-11 |
NDC Item | 70377008211 |
Packaging | 1 BOTTLE, DISPENSING in 1 CARTON (70377-082-11) / 10 mL in 1 BOTTLE, DISPENSING |
ANDA | ANDA202054 |
FDA SPL set id | 611443 |
Labeler | Biocon Pharma Inc. |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2022-01-08 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 70377-082 |
NDC Item 71921022610
NDC 9 | 71921-226 |
---|---|
NDC 10 | 71921-226-10 |
NDC Item | 71921022610 |
Packaging | 1 BOTTLE, DISPENSING in 1 CARTON (71921-226-10) / 10 mL in 1 BOTTLE, DISPENSING |
ANDA | ANDA202054 |
FDA SPL set id | 724181 |
Labeler | Florida Pharmaceutical Products, LLC |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2023-08-16 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 71921-226 |
NDC Item 72162216602
NDC 9 | 72162-2166 |
---|---|
NDC 10 | 72162-2166-2 |
NDC Item | 72162216602 |
Packaging | 1 BOTTLE, DROPPER in 1 CARTON (72162-2166-2) / 10 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA090037 |
FDA SPL set id | 752883 |
Labeler | Bryant Ranch Prepack |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2009-07-14 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 72162-2166 |
NDC Item 72162218402
NDC 9 | 72162-2184 |
---|---|
NDC 10 | 72162-2184-2 |
NDC Item | 72162218402 |
Packaging | 10 mL in 1 BOTTLE (72162-2184-2) |
ANDA | ANDA090604 |
FDA SPL set id | 753279 |
Labeler | Bryant Ranch Prepack |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2010-01-02 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 72162-2184 |
NDC Item 72162238102
NDC 9 | 72162-2381 |
---|---|
NDC 10 | 72162-2381-2 |
NDC Item | 72162238102 |
Packaging | 1 BOTTLE in 1 CARTON (72162-2381-2) / 10 mL in 1 BOTTLE |
ANDA | ANDA204777 |
COLORTEXT | white(colorless to nearly colorless) |
Color | C48325 __ |
FDA SPL set id | 815591 |
Labeler | Bryant Ranch Prepack |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2020-06-15 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 72162-2381 |
NDC Item 00527176373
NDC 9 | 0527-1763 |
---|---|
NDC 10 | 0527-1763-73 |
NDC Item | 00527176373 |
Packaging | 1 BOTTLE, DROPPER in 1 CARTON (0527-1763-73) / 10 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA201998 |
FDA SPL set id | 447745 |
Labeler | Lannett Company, Inc. |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2014-12-17 |
Marketing status | COMPLETED |
Related queries | Properties for NDC 9 0527-1763 |
NDC Item 00781605470
NDC 9 | 0781-6054 |
---|---|
NDC 10 | 0781-6054-70 |
NDC Item | 00781605470 |
Packaging | 1 BOTTLE, DROPPER in 1 CARTON (0781-6054-70) / 10 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA077847 |
Labeler | Sandoz Inc |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing status | COMPLETED |
Related queries | Properties for NDC 9 0781-6054 |
NDC Item 14445040510
NDC 9 | 14445-405 |
---|---|
NDC 10 | 14445-405-10 |
NDC Item | 14445040510 |
Packaging | 1 BOTTLE, DISPENSING in 1 CARTON (14445-405-10) / 10 mL in 1 BOTTLE, DISPENSING |
ANDA | ANDA202054 |
FDA SPL set id | 837670 |
Labeler | Indoco Remedies Limited |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2021-05-14 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 14445-405 |
NDC Item 24208048605
NDC 9 | 24208-486 |
---|---|
NDC 10 | 24208-486-05 |
NDC Item | 24208048605 |
Packaging | 1 BOTTLE, DROPPER in 1 CARTON (24208-486-05) / 5 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA090037 |
FDA SPL set id | 744119 |
Labeler | Bausch & Lomb Incorporated |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2009-07-14 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 24208-486 |
NDC Item 24208048610
NDC 9 | 24208-486 |
---|---|
NDC 10 | 24208-486-10 |
NDC Item | 24208048610 |
Packaging | 1 BOTTLE, DROPPER in 1 CARTON (24208-486-10) / 10 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA090037 |
FDA SPL set id | 744119 |
Labeler | Bausch & Lomb Incorporated |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2009-07-14 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 24208-486 |
NDC Item 42571014726
NDC 9 | 42571-147 |
---|---|
NDC 10 | 42571-147-26 |
NDC Item | 42571014726 |
Packaging | 1 BOTTLE in 1 CARTON (42571-147-26) / 10 mL in 1 BOTTLE |
ANDA | ANDA204777 |
COLORTEXT | white(colorless to nearly colorless) |
Color | C48325 __ |
FDA SPL set id | 812624 |
Labeler | Micro Labs Limited |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2020-06-15 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 42571-147 |
NDC Item 46708055310
NDC 9 | 46708-553 |
---|---|
NDC 10 | 46708-553-10 |
NDC Item | 46708055310 |
Packaging | 1 BOTTLE in 1 CARTON (46708-553-10) / 10 mL in 1 BOTTLE |
ANDA | ANDA213099 |
FDA SPL set id | 827356 |
Labeler | Alembic Pharmaceuticals Limited |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2021-05-04 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 46708-553 |
NDC Item 50090286700
NDC 9 | 50090-2867 |
---|---|
NDC 10 | 50090-2867-0 |
NDC Item | 50090286700 |
Packaging | 1 BOTTLE, DISPENSING in 1 CARTON (50090-2867-0) / 10 mL in 1 BOTTLE, DISPENSING |
ANDA | ANDA202054 |
FDA SPL set id | 302402 |
Labeler | A-S Medication Solutions LLC |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2015-02-17 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 50090-2867 |
NDC Item 50090637100
NDC 9 | 50090-6371 |
---|---|
NDC 10 | 50090-6371-0 |
NDC Item | 50090637100 |
Packaging | 1 BOTTLE, DROPPER in 1 CARTON (50090-6371-0) / 10 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA090037 |
FDA SPL set id | 826332 |
Labeler | A-S Medication Solutions |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2009-07-14 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 50090-6371 |
NDC Item 50090681400
NDC 9 | 50090-6814 |
---|---|
NDC 10 | 50090-6814-0 |
NDC Item | 50090681400 |
Packaging | 1 BOTTLE in 1 CARTON (50090-6814-0) / 10 mL in 1 BOTTLE |
ANDA | ANDA204777 |
COLORTEXT | white(colorless to nearly colorless) |
Color | C48325 __ |
FDA SPL set id | 746492 |
Labeler | A-S Medication Solutions |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2020-06-15 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 50090-6814 |
NDC Item 50383023310
NDC 9 | 50383-233 |
---|---|
NDC 10 | 50383-233-10 |
NDC Item | 50383023310 |
Packaging | 1 BOTTLE, DROPPER in 1 BOX (50383-233-10) / 10 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA077847 |
FDA SPL set id | 640641 |
Labeler | Akorn Operating Company LLC (dba Akorn) |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2008-10-28 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 50383-233 |
NDC Item 60429011510
NDC 9 | 60429-115 |
---|---|
NDC 10 | 60429-115-10 |
NDC Item | 60429011510 |
Packaging | 1 BOTTLE, DROPPER in 1 BOX (60429-115-10) / 10 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA077847 |
FDA SPL set id | 767171 |
Labeler | Golden State Medical Supply, Inc. |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2008-10-28 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 60429-115 |
NDC Item 61314003001
NDC 9 | 61314-030 |
---|---|
NDC 10 | 61314-030-01 |
NDC Item | 61314003001 |
Packaging | 5 mL in 1 BOTTLE (61314-030-01) |
ANDA | ANDA090604 |
FDA SPL set id | 622450 |
Labeler | Sandoz Inc |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2010-01-02 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 61314-030 |
NDC Item 61314003002
NDC 9 | 61314-030 |
---|---|
NDC 10 | 61314-030-02 |
NDC Item | 61314003002 |
Packaging | 10 mL in 1 BOTTLE (61314-030-02) |
ANDA | ANDA090604 |
FDA SPL set id | 622450 |
Labeler | Sandoz Inc |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2010-01-02 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 61314-030 |
NDC Item 62332055310
NDC 9 | 62332-553 |
---|---|
NDC 10 | 62332-553-10 |
NDC Item | 62332055310 |
Packaging | 1 BOTTLE in 1 CARTON (62332-553-10) / 10 mL in 1 BOTTLE |
ANDA | ANDA213099 |
FDA SPL set id | 827411 |
Labeler | Alembic Pharmaceuticals Inc. |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2021-05-04 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 62332-553 |
NDC Item 65862094601
NDC 9 | 65862-946 |
---|---|
NDC 10 | 65862-946-01 |
NDC Item | 65862094601 |
Packaging | 1 BOTTLE, DROPPER in 1 CARTON (65862-946-01) / 10 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA207629 |
FDA SPL set id | 788118 |
Labeler | Aurobindo Pharma Limited |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2021-05-14 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 65862-946 |
NDC Item 68083049001
NDC 9 | 68083-490 |
---|---|
NDC 10 | 68083-490-01 |
NDC Item | 68083049001 |
Packaging | 1 BOTTLE in 1 CARTON (68083-490-01) / 10 mL in 1 BOTTLE |
ANDA | ANDA215520 |
FDA SPL set id | 786662 |
Labeler | Gland Pharma Limited |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2022-09-19 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 68083-490 |
NDC Item 69315030505
NDC 9 | 69315-305 |
---|---|
NDC 10 | 69315-305-05 |
NDC Item | 69315030505 |
Packaging | 1 BOTTLE, PLASTIC in 1 CARTON (69315-305-05) / 5 mL in 1 BOTTLE, PLASTIC |
ANDA | ANDA205295 |
FDA SPL set id | 787995 |
Labeler | Leading Pharma, LLC |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2017-05-18 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 69315-305 |
NDC Item 69315030510
NDC 9 | 69315-305 |
---|---|
NDC 10 | 69315-305-10 |
NDC Item | 69315030510 |
Packaging | 1 BOTTLE, PLASTIC in 1 CARTON (69315-305-10) / 10 mL in 1 BOTTLE, PLASTIC |
ANDA | ANDA205295 |
FDA SPL set id | 787995 |
Labeler | Leading Pharma, LLC |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2017-05-18 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 69315-305 |
NDC Item 70069005101
NDC 9 | 70069-051 |
---|---|
NDC 10 | 70069-051-01 |
NDC Item | 70069005101 |
Packaging | 1 BOTTLE in 1 CARTON (70069-051-01) / 10 mL in 1 BOTTLE |
ANDA | ANDA207523 |
COLORTEXT | WHITE(A clear, colorless to nearly colorless solution) |
Color | C48325 __ |
FDA SPL set id | 755334 |
Labeler | Somerset Therapeutics, LLC |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2019-06-25 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 70069-051 |
NDC Item 70377008211
NDC 9 | 70377-082 |
---|---|
NDC 10 | 70377-082-11 |
NDC Item | 70377008211 |
Packaging | 1 BOTTLE, DISPENSING in 1 CARTON (70377-082-11) / 10 mL in 1 BOTTLE, DISPENSING |
ANDA | ANDA202054 |
FDA SPL set id | 611443 |
Labeler | Biocon Pharma Inc. |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2022-01-08 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 70377-082 |
NDC Item 71921022610
NDC 9 | 71921-226 |
---|---|
NDC 10 | 71921-226-10 |
NDC Item | 71921022610 |
Packaging | 1 BOTTLE, DISPENSING in 1 CARTON (71921-226-10) / 10 mL in 1 BOTTLE, DISPENSING |
ANDA | ANDA202054 |
FDA SPL set id | 724181 |
Labeler | Florida Pharmaceutical Products, LLC |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2023-08-16 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 71921-226 |
NDC Item 72162216602
NDC 9 | 72162-2166 |
---|---|
NDC 10 | 72162-2166-2 |
NDC Item | 72162216602 |
Packaging | 1 BOTTLE, DROPPER in 1 CARTON (72162-2166-2) / 10 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA090037 |
FDA SPL set id | 752883 |
Labeler | Bryant Ranch Prepack |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2009-07-14 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 72162-2166 |
NDC Item 72162218402
NDC 9 | 72162-2184 |
---|---|
NDC 10 | 72162-2184-2 |
NDC Item | 72162218402 |
Packaging | 10 mL in 1 BOTTLE (72162-2184-2) |
ANDA | ANDA090604 |
FDA SPL set id | 753279 |
Labeler | Bryant Ranch Prepack |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2010-01-02 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 72162-2184 |
NDC Item 72162238102
NDC 9 | 72162-2381 |
---|---|
NDC 10 | 72162-2381-2 |
NDC Item | 72162238102 |
Packaging | 1 BOTTLE in 1 CARTON (72162-2381-2) / 10 mL in 1 BOTTLE |
ANDA | ANDA204777 |
COLORTEXT | white(colorless to nearly colorless) |
Color | C48325 __ |
FDA SPL set id | 815591 |
Labeler | Bryant Ranch Prepack |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2020-06-15 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 72162-2381 |
NDC Item 00527176373
NDC 9 | 0527-1763 |
---|---|
NDC 10 | 0527-1763-73 |
NDC Item | 00527176373 |
Packaging | 1 BOTTLE, DROPPER in 1 CARTON (0527-1763-73) / 10 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA201998 |
FDA SPL set id | 447745 |
Labeler | Lannett Company, Inc. |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2014-12-17 |
Marketing status | COMPLETED |
Related queries | Properties for NDC 9 0527-1763 |
NDC Item 00781605470
NDC 9 | 0781-6054 |
---|---|
NDC 10 | 0781-6054-70 |
NDC Item | 00781605470 |
Packaging | 1 BOTTLE, DROPPER in 1 CARTON (0781-6054-70) / 10 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA077847 |
Labeler | Sandoz Inc |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing status | COMPLETED |
Related queries | Properties for NDC 9 0781-6054 |
NDC Item 14445040510
NDC 9 | 14445-405 |
---|---|
NDC 10 | 14445-405-10 |
NDC Item | 14445040510 |
Packaging | 1 BOTTLE, DISPENSING in 1 CARTON (14445-405-10) / 10 mL in 1 BOTTLE, DISPENSING |
ANDA | ANDA202054 |
FDA SPL set id | 837670 |
Labeler | Indoco Remedies Limited |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2021-05-14 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 14445-405 |
NDC Item 24208048605
NDC 9 | 24208-486 |
---|---|
NDC 10 | 24208-486-05 |
NDC Item | 24208048605 |
Packaging | 1 BOTTLE, DROPPER in 1 CARTON (24208-486-05) / 5 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA090037 |
FDA SPL set id | 744119 |
Labeler | Bausch & Lomb Incorporated |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2009-07-14 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 24208-486 |
NDC Item 24208048610
NDC 9 | 24208-486 |
---|---|
NDC 10 | 24208-486-10 |
NDC Item | 24208048610 |
Packaging | 1 BOTTLE, DROPPER in 1 CARTON (24208-486-10) / 10 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA090037 |
FDA SPL set id | 744119 |
Labeler | Bausch & Lomb Incorporated |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2009-07-14 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 24208-486 |
NDC Item 42571014726
NDC 9 | 42571-147 |
---|---|
NDC 10 | 42571-147-26 |
NDC Item | 42571014726 |
Packaging | 1 BOTTLE in 1 CARTON (42571-147-26) / 10 mL in 1 BOTTLE |
ANDA | ANDA204777 |
COLORTEXT | white(colorless to nearly colorless) |
Color | C48325 __ |
FDA SPL set id | 812624 |
Labeler | Micro Labs Limited |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2020-06-15 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 42571-147 |
NDC Item 46708055310
NDC 9 | 46708-553 |
---|---|
NDC 10 | 46708-553-10 |
NDC Item | 46708055310 |
Packaging | 1 BOTTLE in 1 CARTON (46708-553-10) / 10 mL in 1 BOTTLE |
ANDA | ANDA213099 |
FDA SPL set id | 827356 |
Labeler | Alembic Pharmaceuticals Limited |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2021-05-04 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 46708-553 |
NDC Item 50090286700
NDC 9 | 50090-2867 |
---|---|
NDC 10 | 50090-2867-0 |
NDC Item | 50090286700 |
Packaging | 1 BOTTLE, DISPENSING in 1 CARTON (50090-2867-0) / 10 mL in 1 BOTTLE, DISPENSING |
ANDA | ANDA202054 |
FDA SPL set id | 302402 |
Labeler | A-S Medication Solutions LLC |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2015-02-17 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 50090-2867 |
NDC Item 50090637100
NDC 9 | 50090-6371 |
---|---|
NDC 10 | 50090-6371-0 |
NDC Item | 50090637100 |
Packaging | 1 BOTTLE, DROPPER in 1 CARTON (50090-6371-0) / 10 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA090037 |
FDA SPL set id | 826332 |
Labeler | A-S Medication Solutions |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2009-07-14 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 50090-6371 |
NDC Item 50090681400
NDC 9 | 50090-6814 |
---|---|
NDC 10 | 50090-6814-0 |
NDC Item | 50090681400 |
Packaging | 1 BOTTLE in 1 CARTON (50090-6814-0) / 10 mL in 1 BOTTLE |
ANDA | ANDA204777 |
COLORTEXT | white(colorless to nearly colorless) |
Color | C48325 __ |
FDA SPL set id | 746492 |
Labeler | A-S Medication Solutions |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2020-06-15 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 50090-6814 |
NDC Item 50383023310
NDC 9 | 50383-233 |
---|---|
NDC 10 | 50383-233-10 |
NDC Item | 50383023310 |
Packaging | 1 BOTTLE, DROPPER in 1 BOX (50383-233-10) / 10 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA077847 |
FDA SPL set id | 640641 |
Labeler | Akorn Operating Company LLC (dba Akorn) |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2008-10-28 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 50383-233 |
NDC Item 60429011510
NDC 9 | 60429-115 |
---|---|
NDC 10 | 60429-115-10 |
NDC Item | 60429011510 |
Packaging | 1 BOTTLE, DROPPER in 1 BOX (60429-115-10) / 10 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA077847 |
FDA SPL set id | 767171 |
Labeler | Golden State Medical Supply, Inc. |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2008-10-28 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 60429-115 |
NDC Item 61314003001
NDC 9 | 61314-030 |
---|---|
NDC 10 | 61314-030-01 |
NDC Item | 61314003001 |
Packaging | 5 mL in 1 BOTTLE (61314-030-01) |
ANDA | ANDA090604 |
FDA SPL set id | 622450 |
Labeler | Sandoz Inc |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2010-01-02 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 61314-030 |
NDC Item 61314003002
NDC 9 | 61314-030 |
---|---|
NDC 10 | 61314-030-02 |
NDC Item | 61314003002 |
Packaging | 10 mL in 1 BOTTLE (61314-030-02) |
ANDA | ANDA090604 |
FDA SPL set id | 622450 |
Labeler | Sandoz Inc |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2010-01-02 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 61314-030 |
NDC Item 62332055310
NDC 9 | 62332-553 |
---|---|
NDC 10 | 62332-553-10 |
NDC Item | 62332055310 |
Packaging | 1 BOTTLE in 1 CARTON (62332-553-10) / 10 mL in 1 BOTTLE |
ANDA | ANDA213099 |
FDA SPL set id | 827411 |
Labeler | Alembic Pharmaceuticals Inc. |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2021-05-04 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 62332-553 |
NDC Item 65862094601
NDC 9 | 65862-946 |
---|---|
NDC 10 | 65862-946-01 |
NDC Item | 65862094601 |
Packaging | 1 BOTTLE, DROPPER in 1 CARTON (65862-946-01) / 10 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA207629 |
FDA SPL set id | 788118 |
Labeler | Aurobindo Pharma Limited |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2021-05-14 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 65862-946 |
NDC Item 68083049001
NDC 9 | 68083-490 |
---|---|
NDC 10 | 68083-490-01 |
NDC Item | 68083049001 |
Packaging | 1 BOTTLE in 1 CARTON (68083-490-01) / 10 mL in 1 BOTTLE |
ANDA | ANDA215520 |
FDA SPL set id | 786662 |
Labeler | Gland Pharma Limited |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2022-09-19 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 68083-490 |
NDC Item 69315030505
NDC 9 | 69315-305 |
---|---|
NDC 10 | 69315-305-05 |
NDC Item | 69315030505 |
Packaging | 1 BOTTLE, PLASTIC in 1 CARTON (69315-305-05) / 5 mL in 1 BOTTLE, PLASTIC |
ANDA | ANDA205295 |
FDA SPL set id | 787995 |
Labeler | Leading Pharma, LLC |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2017-05-18 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 69315-305 |
NDC Item 69315030510
NDC 9 | 69315-305 |
---|---|
NDC 10 | 69315-305-10 |
NDC Item | 69315030510 |
Packaging | 1 BOTTLE, PLASTIC in 1 CARTON (69315-305-10) / 10 mL in 1 BOTTLE, PLASTIC |
ANDA | ANDA205295 |
FDA SPL set id | 787995 |
Labeler | Leading Pharma, LLC |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2017-05-18 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 69315-305 |
NDC Item 70069005101
NDC 9 | 70069-051 |
---|---|
NDC 10 | 70069-051-01 |
NDC Item | 70069005101 |
Packaging | 1 BOTTLE in 1 CARTON (70069-051-01) / 10 mL in 1 BOTTLE |
ANDA | ANDA207523 |
COLORTEXT | WHITE(A clear, colorless to nearly colorless solution) |
Color | C48325 __ |
FDA SPL set id | 755334 |
Labeler | Somerset Therapeutics, LLC |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2019-06-25 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 70069-051 |
NDC Item 70377008211
NDC 9 | 70377-082 |
---|---|
NDC 10 | 70377-082-11 |
NDC Item | 70377008211 |
Packaging | 1 BOTTLE, DISPENSING in 1 CARTON (70377-082-11) / 10 mL in 1 BOTTLE, DISPENSING |
ANDA | ANDA202054 |
FDA SPL set id | 611443 |
Labeler | Biocon Pharma Inc. |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2022-01-08 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 70377-082 |
NDC Item 71921022610
NDC 9 | 71921-226 |
---|---|
NDC 10 | 71921-226-10 |
NDC Item | 71921022610 |
Packaging | 1 BOTTLE, DISPENSING in 1 CARTON (71921-226-10) / 10 mL in 1 BOTTLE, DISPENSING |
ANDA | ANDA202054 |
FDA SPL set id | 724181 |
Labeler | Florida Pharmaceutical Products, LLC |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2023-08-16 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 71921-226 |
NDC Item 72162216602
NDC 9 | 72162-2166 |
---|---|
NDC 10 | 72162-2166-2 |
NDC Item | 72162216602 |
Packaging | 1 BOTTLE, DROPPER in 1 CARTON (72162-2166-2) / 10 mL in 1 BOTTLE, DROPPER |
ANDA | ANDA090037 |
FDA SPL set id | 752883 |
Labeler | Bryant Ranch Prepack |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2009-07-14 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 72162-2166 |
NDC Item 72162218402
NDC 9 | 72162-2184 |
---|---|
NDC 10 | 72162-2184-2 |
NDC Item | 72162218402 |
Packaging | 10 mL in 1 BOTTLE (72162-2184-2) |
ANDA | ANDA090604 |
FDA SPL set id | 753279 |
Labeler | Bryant Ranch Prepack |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2010-01-02 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 72162-2184 |
NDC Item 72162238102
NDC 9 | 72162-2381 |
---|---|
NDC 10 | 72162-2381-2 |
NDC Item | 72162238102 |
Packaging | 1 BOTTLE in 1 CARTON (72162-2381-2) / 10 mL in 1 BOTTLE |
ANDA | ANDA204777 |
COLORTEXT | white(colorless to nearly colorless) |
Color | C48325 __ |
FDA SPL set id | 815591 |
Labeler | Bryant Ranch Prepack |
Label type | HUMAN PRESCRIPTION DRUG |
Marketing category | ANDA |
Marketing effective time low | 2020-06-15 |
Marketing status | ACTIVE |
Related queries | Properties for NDC 9 72162-2381 |