NDC properties for NDC 9 0527-1763
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 |
| Labeler | Lannett Company, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2014-12-17 |
| Marketing status | COMPLETED |
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 |
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 |
| Labeler | Indoco Remedies Limited |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2021-05-14 |
| Marketing status | ACTIVE |
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 |
| Labeler | Bausch & Lomb Incorporated |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-07-14 |
| Marketing status | ACTIVE |
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 |
| Labeler | Bausch & Lomb Incorporated |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-07-14 |
| Marketing status | ACTIVE |
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 __ |
| Labeler | Micro Labs Limited |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2020-06-15 |
| Marketing status | ACTIVE |
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 |
| Labeler | Alembic Pharmaceuticals Limited |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2021-05-04 |
| Marketing status | ACTIVE |
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 |
| Labeler | A-S Medication Solutions LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2015-02-17 |
| Marketing status | ACTIVE |
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 |
| Labeler | A-S Medication Solutions |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-07-14 |
| Marketing status | ACTIVE |
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 |
| 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 |
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 |
| Labeler | Golden State Medical Supply, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2008-10-28 |
| Marketing status | ACTIVE |
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 |
| Labeler | Sandoz Inc |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-02 |
| Marketing status | ACTIVE |
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 |
| Labeler | Sandoz Inc |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-02 |
| Marketing status | ACTIVE |
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 |
| Labeler | Alembic Pharmaceuticals Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2021-05-04 |
| Marketing status | ACTIVE |
NDC item 64950039060
| NDC 9 | 64950-390 |
|---|---|
| NDC 10 | 64950-390-60 |
| NDC Item | 64950039060 |
| packaging | 60 VIAL, SINGLE-DOSE in 1 CARTON (64950-390-60) / .2 mL in 1 VIAL, SINGLE-DOSE |
| ANDA | ANDA216308 |
| Labeler | Genus Lifesciences |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2025-08-01 |
| Marketing status | ACTIVE |
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 |
| Labeler | Aurobindo Pharma Limited |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2021-05-14 |
| Marketing status | ACTIVE |
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 |
| Labeler | Gland Pharma Limited |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2022-09-19 |
| Marketing status | ACTIVE |
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 |
| Labeler | Leading Pharma, LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2017-05-18 |
| Marketing status | ACTIVE |
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 |
| Labeler | Leading Pharma, LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2017-05-18 |
| Marketing status | ACTIVE |
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 __ |
| Labeler | Somerset Therapeutics, LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2019-06-25 |
| Marketing status | ACTIVE |
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 |
| Labeler | Biocon Pharma Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2022-01-08 |
| Marketing status | ACTIVE |
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 |
| Labeler | Florida Pharmaceutical Products, LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2023-08-16 |
| Marketing status | ACTIVE |
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 |
| Labeler | Bryant Ranch Prepack |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2009-07-14 |
| Marketing status | ACTIVE |
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 |
| Labeler | Bryant Ranch Prepack |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2010-01-02 |
| Marketing status | ACTIVE |
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 __ |
| Labeler | Bryant Ranch Prepack |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2020-06-15 |
| Marketing status | ACTIVE |
NDC item 72603055901
| NDC 9 | 72603-559 |
|---|---|
| NDC 10 | 72603-559-01 |
| NDC Item | 72603055901 |
| packaging | 1 BOTTLE, DROPPER in 1 CARTON (72603-559-01) / 10 mL in 1 BOTTLE, DROPPER |
| ANDA | ANDA207629 |
| Labeler | Northstar RxLLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | ANDA |
| Marketing effective time low | 2025-06-01 |
| Marketing status | ACTIVE |