NDC properties for "TobraDex (dexamethasone 0.1 % / tobramycin 0.3 % ) Ophthalmic Suspension" (RxCUI 208813)
About this data
The tables show NDC propoerties for TobraDex (dexamethasone 0.1 % / tobramycin 0.3 % ) Ophthalmic Suspension with the RxCUI 208813
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 TobraDex (dexamethasone 0.1 % / tobramycin 0.3 % ) Ophthalmic Suspension (RxCUI 208813)
| MMSL_CODE | BD3428 |
|---|---|
| NDA | NDA050592 |
| RxCUI | 208813 |
| SPL_SET_ID | 2a2259ee-05e4-4785-ba75-5946132debf3 |
| SPL_SET_ID | 330ac1f7-d583-454d-96bf-37c5af31a369 |
| SPL_SET_ID | c662bb23-f30c-451d-aa6c-f3f26fb72377 |
| Prescribable Synonym | TobraDex 0.3 % / 0.1 % Ophthalmic Suspension |
| RXNAV_STR | TobraDex (dexAMETHasone 0.1 % / tobramycin 0.3 % ) Ophthalmic Suspension |
| RxNorm Name | dexamethasone 1 MG/ML / tobramycin 3 MG/ML Ophthalmic Suspension [Tobradex] |
| RxNorm Synonym | TobraDex (dexamethasone 0.1 % / tobramycin 0.3 % ) Ophthalmic Suspension |
| Tallman Synonym | dexAMETHasone 1 MG/ML / tobramycin 3 MG/ML Ophthalmic Suspension [Tobradex] |
| Tallman Synonym | TobraDex (dexAMETHasone 0.1 % / tobramycin 0.3 % ) Ophthalmic Suspension |
| Related queries | Interactions (for RxCUI 208813) |
NDC Properties
NDC Item 00065064705
| NDC 9 | 0065-0647 |
|---|---|
| NDC 10 | 0065-0647-05 |
| NDC Item | 00065064705 |
| Packaging | 5 mL in 1 BOTTLE, PLASTIC (0065-0647-05) |
| FDA SPL set id | 692142 |
| Labeler | Alcon Laboratories, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | NDA |
| Marketing effective time high | 2023-08-31 |
| Marketing effective time low | 1988-09-15 |
| Marketing status | COMPLETED |
| NDA | NDA050592 |
| Related queries | Properties for NDC 9 0065-0647 |
NDC Item 00065064710
| NDC 9 | 0065-0647 |
|---|---|
| NDC 10 | 0065-0647-10 |
| NDC Item | 00065064710 |
| Packaging | 10 mL in 1 BOTTLE, PLASTIC (0065-0647-10) |
| FDA SPL set id | 692142 |
| Labeler | Alcon Laboratories, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | NDA |
| Marketing effective time high | 2023-08-31 |
| Marketing effective time low | 1988-09-15 |
| Marketing status | COMPLETED |
| NDA | NDA050592 |
| Related queries | Properties for NDC 9 0065-0647 |
NDC Item 00065064725
| NDC 9 | 0065-0647 |
|---|---|
| NDC 10 | 0065-0647-25 |
| NDC Item | 00065064725 |
| Packaging | 2.5 mL in 1 BOTTLE, PLASTIC (0065-0647-25) |
| FDA SPL set id | 692142 |
| Labeler | Alcon Laboratories, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | NDA |
| Marketing effective time high | 2023-08-31 |
| Marketing effective time low | 1988-09-15 |
| Marketing status | COMPLETED |
| NDA | NDA050592 |
| Related queries | Properties for NDC 9 0065-0647 |
NDC Item 00078095325
| NDC 9 | 0078-0953 |
|---|---|
| NDC 10 | 0078-0953-25 |
| NDC Item | 00078095325 |
| Packaging | 5 mL in 1 BOTTLE (0078-0953-25) |
| FDA SPL set id | 706700 |
| Labeler | Novartis Pharmaceuticals Corporation |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | NDA |
| Marketing effective time low | 1988-09-15 |
| Marketing status | ACTIVE |
| NDA | NDA050592 |
| Related queries | Properties for NDC 9 0078-0953 |
NDC Item 00078095326
| NDC 9 | 0078-0953 |
|---|---|
| NDC 10 | 0078-0953-26 |
| NDC Item | 00078095326 |
| Packaging | 10 mL in 1 BOTTLE (0078-0953-26) |
| FDA SPL set id | 706700 |
| Labeler | Novartis Pharmaceuticals Corporation |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | NDA |
| Marketing effective time low | 1988-09-15 |
| Marketing status | ACTIVE |
| NDA | NDA050592 |
| Related queries | Properties for NDC 9 0078-0953 |
NDC Item 00078095340
| NDC 9 | 0078-0953 |
|---|---|
| NDC 10 | 0078-0953-40 |
| NDC Item | 00078095340 |
| Packaging | 2.5 mL in 1 BOTTLE (0078-0953-40) |
| FDA SPL set id | 706700 |
| Labeler | Novartis Pharmaceuticals Corporation |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | NDA |
| Marketing effective time low | 1988-09-15 |
| Marketing status | ACTIVE |
| NDA | NDA050592 |
| Related queries | Properties for NDC 9 0078-0953 |
NDC Item 43063000501
| NDC 10 | UNKNOWN |
|---|---|
| NDC Item | 43063000501 |
| Related queries | Properties for NDC 9 |
NDC Item 52959009200
| NDC 10 | UNKNOWN |
|---|---|
| NDC Item | 52959009200 |
| Related queries | Properties for NDC 9 |
NDC Item 52959009201
| NDC 10 | UNKNOWN |
|---|---|
| NDC Item | 52959009201 |
| Related queries | Properties for NDC 9 |
NDC Item 52959009203
| NDC 10 | UNKNOWN |
|---|---|
| NDC Item | 52959009203 |
| Related queries | Properties for NDC 9 |
NDC Item 66267093705
| NDC 10 | UNKNOWN |
|---|---|
| NDC Item | 66267093705 |
| Related queries | Properties for NDC 9 |
NDC Item 00065064705
| NDC 9 | 0065-0647 |
|---|---|
| NDC 10 | 0065-0647-05 |
| NDC Item | 00065064705 |
| Packaging | 5 mL in 1 BOTTLE, PLASTIC (0065-0647-05) |
| FDA SPL set id | 692142 |
| Labeler | Alcon Laboratories, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | NDA |
| Marketing effective time high | 2023-08-31 |
| Marketing effective time low | 1988-09-15 |
| Marketing status | COMPLETED |
| NDA | NDA050592 |
| Related queries | Properties for NDC 9 0065-0647 |
NDC Item 00065064710
| NDC 9 | 0065-0647 |
|---|---|
| NDC 10 | 0065-0647-10 |
| NDC Item | 00065064710 |
| Packaging | 10 mL in 1 BOTTLE, PLASTIC (0065-0647-10) |
| FDA SPL set id | 692142 |
| Labeler | Alcon Laboratories, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | NDA |
| Marketing effective time high | 2023-08-31 |
| Marketing effective time low | 1988-09-15 |
| Marketing status | COMPLETED |
| NDA | NDA050592 |
| Related queries | Properties for NDC 9 0065-0647 |
NDC Item 00065064725
| NDC 9 | 0065-0647 |
|---|---|
| NDC 10 | 0065-0647-25 |
| NDC Item | 00065064725 |
| Packaging | 2.5 mL in 1 BOTTLE, PLASTIC (0065-0647-25) |
| FDA SPL set id | 692142 |
| Labeler | Alcon Laboratories, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | NDA |
| Marketing effective time high | 2023-08-31 |
| Marketing effective time low | 1988-09-15 |
| Marketing status | COMPLETED |
| NDA | NDA050592 |
| Related queries | Properties for NDC 9 0065-0647 |
NDC Item 00078095325
| NDC 9 | 0078-0953 |
|---|---|
| NDC 10 | 0078-0953-25 |
| NDC Item | 00078095325 |
| Packaging | 5 mL in 1 BOTTLE (0078-0953-25) |
| FDA SPL set id | 706700 |
| Labeler | Novartis Pharmaceuticals Corporation |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | NDA |
| Marketing effective time low | 1988-09-15 |
| Marketing status | ACTIVE |
| NDA | NDA050592 |
| Related queries | Properties for NDC 9 0078-0953 |
NDC Item 00078095326
| NDC 9 | 0078-0953 |
|---|---|
| NDC 10 | 0078-0953-26 |
| NDC Item | 00078095326 |
| Packaging | 10 mL in 1 BOTTLE (0078-0953-26) |
| FDA SPL set id | 706700 |
| Labeler | Novartis Pharmaceuticals Corporation |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | NDA |
| Marketing effective time low | 1988-09-15 |
| Marketing status | ACTIVE |
| NDA | NDA050592 |
| Related queries | Properties for NDC 9 0078-0953 |
NDC Item 00078095340
| NDC 9 | 0078-0953 |
|---|---|
| NDC 10 | 0078-0953-40 |
| NDC Item | 00078095340 |
| Packaging | 2.5 mL in 1 BOTTLE (0078-0953-40) |
| FDA SPL set id | 706700 |
| Labeler | Novartis Pharmaceuticals Corporation |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | NDA |
| Marketing effective time low | 1988-09-15 |
| Marketing status | ACTIVE |
| NDA | NDA050592 |
| Related queries | Properties for NDC 9 0078-0953 |
NDC Item 43063000501
| NDC 10 | UNKNOWN |
|---|---|
| NDC Item | 43063000501 |
| Related queries | Properties for NDC 9 |
NDC Item 52959009200
| NDC 10 | UNKNOWN |
|---|---|
| NDC Item | 52959009200 |
| Related queries | Properties for NDC 9 |
NDC Item 52959009201
| NDC 10 | UNKNOWN |
|---|---|
| NDC Item | 52959009201 |
| Related queries | Properties for NDC 9 |
NDC Item 52959009203
| NDC 10 | UNKNOWN |
|---|---|
| NDC Item | 52959009203 |
| Related queries | Properties for NDC 9 |
NDC Item 66267093705
| NDC 10 | UNKNOWN |
|---|---|
| NDC Item | 66267093705 |
| Related queries | Properties for NDC 9 |
NDC Item 00065064705
| NDC 9 | 0065-0647 |
|---|---|
| NDC 10 | 0065-0647-05 |
| NDC Item | 00065064705 |
| Packaging | 5 mL in 1 BOTTLE, PLASTIC (0065-0647-05) |
| FDA SPL set id | 692142 |
| Labeler | Alcon Laboratories, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | NDA |
| Marketing effective time high | 2023-08-31 |
| Marketing effective time low | 1988-09-15 |
| Marketing status | COMPLETED |
| NDA | NDA050592 |
| Related queries | Properties for NDC 9 0065-0647 |
NDC Item 00065064710
| NDC 9 | 0065-0647 |
|---|---|
| NDC 10 | 0065-0647-10 |
| NDC Item | 00065064710 |
| Packaging | 10 mL in 1 BOTTLE, PLASTIC (0065-0647-10) |
| FDA SPL set id | 692142 |
| Labeler | Alcon Laboratories, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | NDA |
| Marketing effective time high | 2023-08-31 |
| Marketing effective time low | 1988-09-15 |
| Marketing status | COMPLETED |
| NDA | NDA050592 |
| Related queries | Properties for NDC 9 0065-0647 |
NDC Item 00065064725
| NDC 9 | 0065-0647 |
|---|---|
| NDC 10 | 0065-0647-25 |
| NDC Item | 00065064725 |
| Packaging | 2.5 mL in 1 BOTTLE, PLASTIC (0065-0647-25) |
| FDA SPL set id | 692142 |
| Labeler | Alcon Laboratories, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | NDA |
| Marketing effective time high | 2023-08-31 |
| Marketing effective time low | 1988-09-15 |
| Marketing status | COMPLETED |
| NDA | NDA050592 |
| Related queries | Properties for NDC 9 0065-0647 |
NDC Item 00078095325
| NDC 9 | 0078-0953 |
|---|---|
| NDC 10 | 0078-0953-25 |
| NDC Item | 00078095325 |
| Packaging | 5 mL in 1 BOTTLE (0078-0953-25) |
| FDA SPL set id | 706700 |
| Labeler | Novartis Pharmaceuticals Corporation |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | NDA |
| Marketing effective time low | 1988-09-15 |
| Marketing status | ACTIVE |
| NDA | NDA050592 |
| Related queries | Properties for NDC 9 0078-0953 |
NDC Item 00078095326
| NDC 9 | 0078-0953 |
|---|---|
| NDC 10 | 0078-0953-26 |
| NDC Item | 00078095326 |
| Packaging | 10 mL in 1 BOTTLE (0078-0953-26) |
| FDA SPL set id | 706700 |
| Labeler | Novartis Pharmaceuticals Corporation |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | NDA |
| Marketing effective time low | 1988-09-15 |
| Marketing status | ACTIVE |
| NDA | NDA050592 |
| Related queries | Properties for NDC 9 0078-0953 |
NDC Item 00078095340
| NDC 9 | 0078-0953 |
|---|---|
| NDC 10 | 0078-0953-40 |
| NDC Item | 00078095340 |
| Packaging | 2.5 mL in 1 BOTTLE (0078-0953-40) |
| FDA SPL set id | 706700 |
| Labeler | Novartis Pharmaceuticals Corporation |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | NDA |
| Marketing effective time low | 1988-09-15 |
| Marketing status | ACTIVE |
| NDA | NDA050592 |
| Related queries | Properties for NDC 9 0078-0953 |
NDC Item 43063000501
| NDC 10 | UNKNOWN |
|---|---|
| NDC Item | 43063000501 |
| Related queries | Properties for NDC 9 |
NDC Item 52959009200
| NDC 10 | UNKNOWN |
|---|---|
| NDC Item | 52959009200 |
| Related queries | Properties for NDC 9 |
NDC Item 52959009201
| NDC 10 | UNKNOWN |
|---|---|
| NDC Item | 52959009201 |
| Related queries | Properties for NDC 9 |
NDC Item 52959009203
| NDC 10 | UNKNOWN |
|---|---|
| NDC Item | 52959009203 |
| Related queries | Properties for NDC 9 |
NDC Item 66267093705
| NDC 10 | UNKNOWN |
|---|---|
| NDC Item | 66267093705 |
| Related queries | Properties for NDC 9 |
NDC Item 00065064705
| NDC 9 | 0065-0647 |
|---|---|
| NDC 10 | 0065-0647-05 |
| NDC Item | 00065064705 |
| Packaging | 5 mL in 1 BOTTLE, PLASTIC (0065-0647-05) |
| FDA SPL set id | 692142 |
| Labeler | Alcon Laboratories, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | NDA |
| Marketing effective time high | 2023-08-31 |
| Marketing effective time low | 1988-09-15 |
| Marketing status | COMPLETED |
| NDA | NDA050592 |
| Related queries | Properties for NDC 9 0065-0647 |
NDC Item 00065064710
| NDC 9 | 0065-0647 |
|---|---|
| NDC 10 | 0065-0647-10 |
| NDC Item | 00065064710 |
| Packaging | 10 mL in 1 BOTTLE, PLASTIC (0065-0647-10) |
| FDA SPL set id | 692142 |
| Labeler | Alcon Laboratories, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | NDA |
| Marketing effective time high | 2023-08-31 |
| Marketing effective time low | 1988-09-15 |
| Marketing status | COMPLETED |
| NDA | NDA050592 |
| Related queries | Properties for NDC 9 0065-0647 |
NDC Item 00065064725
| NDC 9 | 0065-0647 |
|---|---|
| NDC 10 | 0065-0647-25 |
| NDC Item | 00065064725 |
| Packaging | 2.5 mL in 1 BOTTLE, PLASTIC (0065-0647-25) |
| FDA SPL set id | 692142 |
| Labeler | Alcon Laboratories, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | NDA |
| Marketing effective time high | 2023-08-31 |
| Marketing effective time low | 1988-09-15 |
| Marketing status | COMPLETED |
| NDA | NDA050592 |
| Related queries | Properties for NDC 9 0065-0647 |
NDC Item 00078095325
| NDC 9 | 0078-0953 |
|---|---|
| NDC 10 | 0078-0953-25 |
| NDC Item | 00078095325 |
| Packaging | 5 mL in 1 BOTTLE (0078-0953-25) |
| FDA SPL set id | 706700 |
| Labeler | Novartis Pharmaceuticals Corporation |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | NDA |
| Marketing effective time low | 1988-09-15 |
| Marketing status | ACTIVE |
| NDA | NDA050592 |
| Related queries | Properties for NDC 9 0078-0953 |
NDC Item 00078095326
| NDC 9 | 0078-0953 |
|---|---|
| NDC 10 | 0078-0953-26 |
| NDC Item | 00078095326 |
| Packaging | 10 mL in 1 BOTTLE (0078-0953-26) |
| FDA SPL set id | 706700 |
| Labeler | Novartis Pharmaceuticals Corporation |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | NDA |
| Marketing effective time low | 1988-09-15 |
| Marketing status | ACTIVE |
| NDA | NDA050592 |
| Related queries | Properties for NDC 9 0078-0953 |
NDC Item 00078095340
| NDC 9 | 0078-0953 |
|---|---|
| NDC 10 | 0078-0953-40 |
| NDC Item | 00078095340 |
| Packaging | 2.5 mL in 1 BOTTLE (0078-0953-40) |
| FDA SPL set id | 706700 |
| Labeler | Novartis Pharmaceuticals Corporation |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | NDA |
| Marketing effective time low | 1988-09-15 |
| Marketing status | ACTIVE |
| NDA | NDA050592 |
| Related queries | Properties for NDC 9 0078-0953 |
NDC Item 43063000501
| NDC 10 | UNKNOWN |
|---|---|
| NDC Item | 43063000501 |
| Related queries | Properties for NDC 9 |
NDC Item 52959009200
| NDC 10 | UNKNOWN |
|---|---|
| NDC Item | 52959009200 |
| Related queries | Properties for NDC 9 |
NDC Item 52959009201
| NDC 10 | UNKNOWN |
|---|---|
| NDC Item | 52959009201 |
| Related queries | Properties for NDC 9 |
NDC Item 52959009203
| NDC 10 | UNKNOWN |
|---|---|
| NDC Item | 52959009203 |
| Related queries | Properties for NDC 9 |
NDC Item 66267093705
| NDC 10 | UNKNOWN |
|---|---|
| NDC Item | 66267093705 |
| Related queries | Properties for NDC 9 |
NDC Item 00065064705
| NDC 9 | 0065-0647 |
|---|---|
| NDC 10 | 0065-0647-05 |
| NDC Item | 00065064705 |
| Packaging | 5 mL in 1 BOTTLE, PLASTIC (0065-0647-05) |
| FDA SPL set id | 692142 |
| Labeler | Alcon Laboratories, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | NDA |
| Marketing effective time high | 2023-08-31 |
| Marketing effective time low | 1988-09-15 |
| Marketing status | COMPLETED |
| NDA | NDA050592 |
| Related queries | Properties for NDC 9 0065-0647 |
NDC Item 00065064710
| NDC 9 | 0065-0647 |
|---|---|
| NDC 10 | 0065-0647-10 |
| NDC Item | 00065064710 |
| Packaging | 10 mL in 1 BOTTLE, PLASTIC (0065-0647-10) |
| FDA SPL set id | 692142 |
| Labeler | Alcon Laboratories, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | NDA |
| Marketing effective time high | 2023-08-31 |
| Marketing effective time low | 1988-09-15 |
| Marketing status | COMPLETED |
| NDA | NDA050592 |
| Related queries | Properties for NDC 9 0065-0647 |
NDC Item 00065064725
| NDC 9 | 0065-0647 |
|---|---|
| NDC 10 | 0065-0647-25 |
| NDC Item | 00065064725 |
| Packaging | 2.5 mL in 1 BOTTLE, PLASTIC (0065-0647-25) |
| FDA SPL set id | 692142 |
| Labeler | Alcon Laboratories, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | NDA |
| Marketing effective time high | 2023-08-31 |
| Marketing effective time low | 1988-09-15 |
| Marketing status | COMPLETED |
| NDA | NDA050592 |
| Related queries | Properties for NDC 9 0065-0647 |
NDC Item 00078095325
| NDC 9 | 0078-0953 |
|---|---|
| NDC 10 | 0078-0953-25 |
| NDC Item | 00078095325 |
| Packaging | 5 mL in 1 BOTTLE (0078-0953-25) |
| FDA SPL set id | 706700 |
| Labeler | Novartis Pharmaceuticals Corporation |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | NDA |
| Marketing effective time low | 1988-09-15 |
| Marketing status | ACTIVE |
| NDA | NDA050592 |
| Related queries | Properties for NDC 9 0078-0953 |
NDC Item 00078095326
| NDC 9 | 0078-0953 |
|---|---|
| NDC 10 | 0078-0953-26 |
| NDC Item | 00078095326 |
| Packaging | 10 mL in 1 BOTTLE (0078-0953-26) |
| FDA SPL set id | 706700 |
| Labeler | Novartis Pharmaceuticals Corporation |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | NDA |
| Marketing effective time low | 1988-09-15 |
| Marketing status | ACTIVE |
| NDA | NDA050592 |
| Related queries | Properties for NDC 9 0078-0953 |
NDC Item 00078095340
| NDC 9 | 0078-0953 |
|---|---|
| NDC 10 | 0078-0953-40 |
| NDC Item | 00078095340 |
| Packaging | 2.5 mL in 1 BOTTLE (0078-0953-40) |
| FDA SPL set id | 706700 |
| Labeler | Novartis Pharmaceuticals Corporation |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | NDA |
| Marketing effective time low | 1988-09-15 |
| Marketing status | ACTIVE |
| NDA | NDA050592 |
| Related queries | Properties for NDC 9 0078-0953 |
NDC Item 43063000501
| NDC 10 | UNKNOWN |
|---|---|
| NDC Item | 43063000501 |
| Related queries | Properties for NDC 9 |
NDC Item 52959009200
| NDC 10 | UNKNOWN |
|---|---|
| NDC Item | 52959009200 |
| Related queries | Properties for NDC 9 |
NDC Item 52959009201
| NDC 10 | UNKNOWN |
|---|---|
| NDC Item | 52959009201 |
| Related queries | Properties for NDC 9 |
NDC Item 52959009203
| NDC 10 | UNKNOWN |
|---|---|
| NDC Item | 52959009203 |
| Related queries | Properties for NDC 9 |
NDC Item 66267093705
| NDC 10 | UNKNOWN |
|---|---|
| NDC Item | 66267093705 |
| Related queries | Properties for NDC 9 |
NDC Item 00065064705
| NDC 9 | 0065-0647 |
|---|---|
| NDC 10 | 0065-0647-05 |
| NDC Item | 00065064705 |
| Packaging | 5 mL in 1 BOTTLE, PLASTIC (0065-0647-05) |
| FDA SPL set id | 692142 |
| Labeler | Alcon Laboratories, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | NDA |
| Marketing effective time high | 2023-08-31 |
| Marketing effective time low | 1988-09-15 |
| Marketing status | COMPLETED |
| NDA | NDA050592 |
| Related queries | Properties for NDC 9 0065-0647 |
NDC Item 00065064710
| NDC 9 | 0065-0647 |
|---|---|
| NDC 10 | 0065-0647-10 |
| NDC Item | 00065064710 |
| Packaging | 10 mL in 1 BOTTLE, PLASTIC (0065-0647-10) |
| FDA SPL set id | 692142 |
| Labeler | Alcon Laboratories, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | NDA |
| Marketing effective time high | 2023-08-31 |
| Marketing effective time low | 1988-09-15 |
| Marketing status | COMPLETED |
| NDA | NDA050592 |
| Related queries | Properties for NDC 9 0065-0647 |
NDC Item 00065064725
| NDC 9 | 0065-0647 |
|---|---|
| NDC 10 | 0065-0647-25 |
| NDC Item | 00065064725 |
| Packaging | 2.5 mL in 1 BOTTLE, PLASTIC (0065-0647-25) |
| FDA SPL set id | 692142 |
| Labeler | Alcon Laboratories, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | NDA |
| Marketing effective time high | 2023-08-31 |
| Marketing effective time low | 1988-09-15 |
| Marketing status | COMPLETED |
| NDA | NDA050592 |
| Related queries | Properties for NDC 9 0065-0647 |
NDC Item 00078095325
| NDC 9 | 0078-0953 |
|---|---|
| NDC 10 | 0078-0953-25 |
| NDC Item | 00078095325 |
| Packaging | 5 mL in 1 BOTTLE (0078-0953-25) |
| FDA SPL set id | 706700 |
| Labeler | Novartis Pharmaceuticals Corporation |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | NDA |
| Marketing effective time low | 1988-09-15 |
| Marketing status | ACTIVE |
| NDA | NDA050592 |
| Related queries | Properties for NDC 9 0078-0953 |
NDC Item 00078095326
| NDC 9 | 0078-0953 |
|---|---|
| NDC 10 | 0078-0953-26 |
| NDC Item | 00078095326 |
| Packaging | 10 mL in 1 BOTTLE (0078-0953-26) |
| FDA SPL set id | 706700 |
| Labeler | Novartis Pharmaceuticals Corporation |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | NDA |
| Marketing effective time low | 1988-09-15 |
| Marketing status | ACTIVE |
| NDA | NDA050592 |
| Related queries | Properties for NDC 9 0078-0953 |
NDC Item 00078095340
| NDC 9 | 0078-0953 |
|---|---|
| NDC 10 | 0078-0953-40 |
| NDC Item | 00078095340 |
| Packaging | 2.5 mL in 1 BOTTLE (0078-0953-40) |
| FDA SPL set id | 706700 |
| Labeler | Novartis Pharmaceuticals Corporation |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | NDA |
| Marketing effective time low | 1988-09-15 |
| Marketing status | ACTIVE |
| NDA | NDA050592 |
| Related queries | Properties for NDC 9 0078-0953 |
NDC Item 43063000501
| NDC 10 | UNKNOWN |
|---|---|
| NDC Item | 43063000501 |
| Related queries | Properties for NDC 9 |
NDC Item 52959009200
| NDC 10 | UNKNOWN |
|---|---|
| NDC Item | 52959009200 |
| Related queries | Properties for NDC 9 |
NDC Item 52959009201
| NDC 10 | UNKNOWN |
|---|---|
| NDC Item | 52959009201 |
| Related queries | Properties for NDC 9 |
NDC Item 52959009203
| NDC 10 | UNKNOWN |
|---|---|
| NDC Item | 52959009203 |
| Related queries | Properties for NDC 9 |
NDC Item 66267093705
| NDC 10 | UNKNOWN |
|---|---|
| NDC Item | 66267093705 |
| Related queries | Properties for NDC 9 |
NDC Item 00065064705
| NDC 9 | 0065-0647 |
|---|---|
| NDC 10 | 0065-0647-05 |
| NDC Item | 00065064705 |
| Packaging | 5 mL in 1 BOTTLE, PLASTIC (0065-0647-05) |
| FDA SPL set id | 692142 |
| Labeler | Alcon Laboratories, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | NDA |
| Marketing effective time high | 2023-08-31 |
| Marketing effective time low | 1988-09-15 |
| Marketing status | COMPLETED |
| NDA | NDA050592 |
| Related queries | Properties for NDC 9 0065-0647 |
NDC Item 00065064710
| NDC 9 | 0065-0647 |
|---|---|
| NDC 10 | 0065-0647-10 |
| NDC Item | 00065064710 |
| Packaging | 10 mL in 1 BOTTLE, PLASTIC (0065-0647-10) |
| FDA SPL set id | 692142 |
| Labeler | Alcon Laboratories, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | NDA |
| Marketing effective time high | 2023-08-31 |
| Marketing effective time low | 1988-09-15 |
| Marketing status | COMPLETED |
| NDA | NDA050592 |
| Related queries | Properties for NDC 9 0065-0647 |
NDC Item 00065064725
| NDC 9 | 0065-0647 |
|---|---|
| NDC 10 | 0065-0647-25 |
| NDC Item | 00065064725 |
| Packaging | 2.5 mL in 1 BOTTLE, PLASTIC (0065-0647-25) |
| FDA SPL set id | 692142 |
| Labeler | Alcon Laboratories, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | NDA |
| Marketing effective time high | 2023-08-31 |
| Marketing effective time low | 1988-09-15 |
| Marketing status | COMPLETED |
| NDA | NDA050592 |
| Related queries | Properties for NDC 9 0065-0647 |
NDC Item 00078095325
| NDC 9 | 0078-0953 |
|---|---|
| NDC 10 | 0078-0953-25 |
| NDC Item | 00078095325 |
| Packaging | 5 mL in 1 BOTTLE (0078-0953-25) |
| FDA SPL set id | 706700 |
| Labeler | Novartis Pharmaceuticals Corporation |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | NDA |
| Marketing effective time low | 1988-09-15 |
| Marketing status | ACTIVE |
| NDA | NDA050592 |
| Related queries | Properties for NDC 9 0078-0953 |
NDC Item 00078095326
| NDC 9 | 0078-0953 |
|---|---|
| NDC 10 | 0078-0953-26 |
| NDC Item | 00078095326 |
| Packaging | 10 mL in 1 BOTTLE (0078-0953-26) |
| FDA SPL set id | 706700 |
| Labeler | Novartis Pharmaceuticals Corporation |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | NDA |
| Marketing effective time low | 1988-09-15 |
| Marketing status | ACTIVE |
| NDA | NDA050592 |
| Related queries | Properties for NDC 9 0078-0953 |
NDC Item 00078095340
| NDC 9 | 0078-0953 |
|---|---|
| NDC 10 | 0078-0953-40 |
| NDC Item | 00078095340 |
| Packaging | 2.5 mL in 1 BOTTLE (0078-0953-40) |
| FDA SPL set id | 706700 |
| Labeler | Novartis Pharmaceuticals Corporation |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | NDA |
| Marketing effective time low | 1988-09-15 |
| Marketing status | ACTIVE |
| NDA | NDA050592 |
| Related queries | Properties for NDC 9 0078-0953 |
NDC Item 43063000501
| NDC 10 | UNKNOWN |
|---|---|
| NDC Item | 43063000501 |
| Related queries | Properties for NDC 9 |
NDC Item 52959009200
| NDC 10 | UNKNOWN |
|---|---|
| NDC Item | 52959009200 |
| Related queries | Properties for NDC 9 |
NDC Item 52959009201
| NDC 10 | UNKNOWN |
|---|---|
| NDC Item | 52959009201 |
| Related queries | Properties for NDC 9 |
NDC Item 52959009203
| NDC 10 | UNKNOWN |
|---|---|
| NDC Item | 52959009203 |
| Related queries | Properties for NDC 9 |
NDC Item 66267093705
| NDC 10 | UNKNOWN |
|---|---|
| NDC Item | 66267093705 |
| Related queries | Properties for NDC 9 |
NDC Item 00065064705
| NDC 9 | 0065-0647 |
|---|---|
| NDC 10 | 0065-0647-05 |
| NDC Item | 00065064705 |
| Packaging | 5 mL in 1 BOTTLE, PLASTIC (0065-0647-05) |
| FDA SPL set id | 692142 |
| Labeler | Alcon Laboratories, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | NDA |
| Marketing effective time high | 2023-08-31 |
| Marketing effective time low | 1988-09-15 |
| Marketing status | COMPLETED |
| NDA | NDA050592 |
| Related queries | Properties for NDC 9 0065-0647 |
NDC Item 00065064710
| NDC 9 | 0065-0647 |
|---|---|
| NDC 10 | 0065-0647-10 |
| NDC Item | 00065064710 |
| Packaging | 10 mL in 1 BOTTLE, PLASTIC (0065-0647-10) |
| FDA SPL set id | 692142 |
| Labeler | Alcon Laboratories, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | NDA |
| Marketing effective time high | 2023-08-31 |
| Marketing effective time low | 1988-09-15 |
| Marketing status | COMPLETED |
| NDA | NDA050592 |
| Related queries | Properties for NDC 9 0065-0647 |
NDC Item 00065064725
| NDC 9 | 0065-0647 |
|---|---|
| NDC 10 | 0065-0647-25 |
| NDC Item | 00065064725 |
| Packaging | 2.5 mL in 1 BOTTLE, PLASTIC (0065-0647-25) |
| FDA SPL set id | 692142 |
| Labeler | Alcon Laboratories, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | NDA |
| Marketing effective time high | 2023-08-31 |
| Marketing effective time low | 1988-09-15 |
| Marketing status | COMPLETED |
| NDA | NDA050592 |
| Related queries | Properties for NDC 9 0065-0647 |
NDC Item 00078095325
| NDC 9 | 0078-0953 |
|---|---|
| NDC 10 | 0078-0953-25 |
| NDC Item | 00078095325 |
| Packaging | 5 mL in 1 BOTTLE (0078-0953-25) |
| FDA SPL set id | 706700 |
| Labeler | Novartis Pharmaceuticals Corporation |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | NDA |
| Marketing effective time low | 1988-09-15 |
| Marketing status | ACTIVE |
| NDA | NDA050592 |
| Related queries | Properties for NDC 9 0078-0953 |
NDC Item 00078095326
| NDC 9 | 0078-0953 |
|---|---|
| NDC 10 | 0078-0953-26 |
| NDC Item | 00078095326 |
| Packaging | 10 mL in 1 BOTTLE (0078-0953-26) |
| FDA SPL set id | 706700 |
| Labeler | Novartis Pharmaceuticals Corporation |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | NDA |
| Marketing effective time low | 1988-09-15 |
| Marketing status | ACTIVE |
| NDA | NDA050592 |
| Related queries | Properties for NDC 9 0078-0953 |
NDC Item 00078095340
| NDC 9 | 0078-0953 |
|---|---|
| NDC 10 | 0078-0953-40 |
| NDC Item | 00078095340 |
| Packaging | 2.5 mL in 1 BOTTLE (0078-0953-40) |
| FDA SPL set id | 706700 |
| Labeler | Novartis Pharmaceuticals Corporation |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | NDA |
| Marketing effective time low | 1988-09-15 |
| Marketing status | ACTIVE |
| NDA | NDA050592 |
| Related queries | Properties for NDC 9 0078-0953 |
NDC Item 43063000501
| NDC 10 | UNKNOWN |
|---|---|
| NDC Item | 43063000501 |
| Related queries | Properties for NDC 9 |
NDC Item 52959009200
| NDC 10 | UNKNOWN |
|---|---|
| NDC Item | 52959009200 |
| Related queries | Properties for NDC 9 |
NDC Item 52959009201
| NDC 10 | UNKNOWN |
|---|---|
| NDC Item | 52959009201 |
| Related queries | Properties for NDC 9 |
NDC Item 52959009203
| NDC 10 | UNKNOWN |
|---|---|
| NDC Item | 52959009203 |
| Related queries | Properties for NDC 9 |
NDC Item 66267093705
| NDC 10 | UNKNOWN |
|---|---|
| NDC Item | 66267093705 |
| Related queries | Properties for NDC 9 |
NDC Item 00065064705
| NDC 9 | 0065-0647 |
|---|---|
| NDC 10 | 0065-0647-05 |
| NDC Item | 00065064705 |
| Packaging | 5 mL in 1 BOTTLE, PLASTIC (0065-0647-05) |
| FDA SPL set id | 692142 |
| Labeler | Alcon Laboratories, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | NDA |
| Marketing effective time high | 2023-08-31 |
| Marketing effective time low | 1988-09-15 |
| Marketing status | COMPLETED |
| NDA | NDA050592 |
| Related queries | Properties for NDC 9 0065-0647 |
NDC Item 00065064710
| NDC 9 | 0065-0647 |
|---|---|
| NDC 10 | 0065-0647-10 |
| NDC Item | 00065064710 |
| Packaging | 10 mL in 1 BOTTLE, PLASTIC (0065-0647-10) |
| FDA SPL set id | 692142 |
| Labeler | Alcon Laboratories, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | NDA |
| Marketing effective time high | 2023-08-31 |
| Marketing effective time low | 1988-09-15 |
| Marketing status | COMPLETED |
| NDA | NDA050592 |
| Related queries | Properties for NDC 9 0065-0647 |
NDC Item 00065064725
| NDC 9 | 0065-0647 |
|---|---|
| NDC 10 | 0065-0647-25 |
| NDC Item | 00065064725 |
| Packaging | 2.5 mL in 1 BOTTLE, PLASTIC (0065-0647-25) |
| FDA SPL set id | 692142 |
| Labeler | Alcon Laboratories, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | NDA |
| Marketing effective time high | 2023-08-31 |
| Marketing effective time low | 1988-09-15 |
| Marketing status | COMPLETED |
| NDA | NDA050592 |
| Related queries | Properties for NDC 9 0065-0647 |
NDC Item 00078095325
| NDC 9 | 0078-0953 |
|---|---|
| NDC 10 | 0078-0953-25 |
| NDC Item | 00078095325 |
| Packaging | 5 mL in 1 BOTTLE (0078-0953-25) |
| FDA SPL set id | 706700 |
| Labeler | Novartis Pharmaceuticals Corporation |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | NDA |
| Marketing effective time low | 1988-09-15 |
| Marketing status | ACTIVE |
| NDA | NDA050592 |
| Related queries | Properties for NDC 9 0078-0953 |
NDC Item 00078095326
| NDC 9 | 0078-0953 |
|---|---|
| NDC 10 | 0078-0953-26 |
| NDC Item | 00078095326 |
| Packaging | 10 mL in 1 BOTTLE (0078-0953-26) |
| FDA SPL set id | 706700 |
| Labeler | Novartis Pharmaceuticals Corporation |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | NDA |
| Marketing effective time low | 1988-09-15 |
| Marketing status | ACTIVE |
| NDA | NDA050592 |
| Related queries | Properties for NDC 9 0078-0953 |
NDC Item 00078095340
| NDC 9 | 0078-0953 |
|---|---|
| NDC 10 | 0078-0953-40 |
| NDC Item | 00078095340 |
| Packaging | 2.5 mL in 1 BOTTLE (0078-0953-40) |
| FDA SPL set id | 706700 |
| Labeler | Novartis Pharmaceuticals Corporation |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | NDA |
| Marketing effective time low | 1988-09-15 |
| Marketing status | ACTIVE |
| NDA | NDA050592 |
| Related queries | Properties for NDC 9 0078-0953 |
NDC Item 43063000501
| NDC 10 | UNKNOWN |
|---|---|
| NDC Item | 43063000501 |
| Related queries | Properties for NDC 9 |
NDC Item 52959009200
| NDC 10 | UNKNOWN |
|---|---|
| NDC Item | 52959009200 |
| Related queries | Properties for NDC 9 |
NDC Item 52959009201
| NDC 10 | UNKNOWN |
|---|---|
| NDC Item | 52959009201 |
| Related queries | Properties for NDC 9 |
NDC Item 52959009203
| NDC 10 | UNKNOWN |
|---|---|
| NDC Item | 52959009203 |
| Related queries | Properties for NDC 9 |
NDC Item 66267093705
| NDC 10 | UNKNOWN |
|---|---|
| NDC Item | 66267093705 |
| Related queries | Properties for NDC 9 |
NDC Item 00065064705
| NDC 9 | 0065-0647 |
|---|---|
| NDC 10 | 0065-0647-05 |
| NDC Item | 00065064705 |
| Packaging | 5 mL in 1 BOTTLE, PLASTIC (0065-0647-05) |
| FDA SPL set id | 692142 |
| Labeler | Alcon Laboratories, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | NDA |
| Marketing effective time high | 2023-08-31 |
| Marketing effective time low | 1988-09-15 |
| Marketing status | COMPLETED |
| NDA | NDA050592 |
| Related queries | Properties for NDC 9 0065-0647 |
NDC Item 00065064710
| NDC 9 | 0065-0647 |
|---|---|
| NDC 10 | 0065-0647-10 |
| NDC Item | 00065064710 |
| Packaging | 10 mL in 1 BOTTLE, PLASTIC (0065-0647-10) |
| FDA SPL set id | 692142 |
| Labeler | Alcon Laboratories, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | NDA |
| Marketing effective time high | 2023-08-31 |
| Marketing effective time low | 1988-09-15 |
| Marketing status | COMPLETED |
| NDA | NDA050592 |
| Related queries | Properties for NDC 9 0065-0647 |
NDC Item 00065064725
| NDC 9 | 0065-0647 |
|---|---|
| NDC 10 | 0065-0647-25 |
| NDC Item | 00065064725 |
| Packaging | 2.5 mL in 1 BOTTLE, PLASTIC (0065-0647-25) |
| FDA SPL set id | 692142 |
| Labeler | Alcon Laboratories, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | NDA |
| Marketing effective time high | 2023-08-31 |
| Marketing effective time low | 1988-09-15 |
| Marketing status | COMPLETED |
| NDA | NDA050592 |
| Related queries | Properties for NDC 9 0065-0647 |
NDC Item 00078095325
| NDC 9 | 0078-0953 |
|---|---|
| NDC 10 | 0078-0953-25 |
| NDC Item | 00078095325 |
| Packaging | 5 mL in 1 BOTTLE (0078-0953-25) |
| FDA SPL set id | 706700 |
| Labeler | Novartis Pharmaceuticals Corporation |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | NDA |
| Marketing effective time low | 1988-09-15 |
| Marketing status | ACTIVE |
| NDA | NDA050592 |
| Related queries | Properties for NDC 9 0078-0953 |
NDC Item 00078095326
| NDC 9 | 0078-0953 |
|---|---|
| NDC 10 | 0078-0953-26 |
| NDC Item | 00078095326 |
| Packaging | 10 mL in 1 BOTTLE (0078-0953-26) |
| FDA SPL set id | 706700 |
| Labeler | Novartis Pharmaceuticals Corporation |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | NDA |
| Marketing effective time low | 1988-09-15 |
| Marketing status | ACTIVE |
| NDA | NDA050592 |
| Related queries | Properties for NDC 9 0078-0953 |
NDC Item 00078095340
| NDC 9 | 0078-0953 |
|---|---|
| NDC 10 | 0078-0953-40 |
| NDC Item | 00078095340 |
| Packaging | 2.5 mL in 1 BOTTLE (0078-0953-40) |
| FDA SPL set id | 706700 |
| Labeler | Novartis Pharmaceuticals Corporation |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | NDA |
| Marketing effective time low | 1988-09-15 |
| Marketing status | ACTIVE |
| NDA | NDA050592 |
| Related queries | Properties for NDC 9 0078-0953 |
NDC Item 43063000501
| NDC 10 | UNKNOWN |
|---|---|
| NDC Item | 43063000501 |
| Related queries | Properties for NDC 9 |
NDC Item 52959009200
| NDC 10 | UNKNOWN |
|---|---|
| NDC Item | 52959009200 |
| Related queries | Properties for NDC 9 |
NDC Item 52959009201
| NDC 10 | UNKNOWN |
|---|---|
| NDC Item | 52959009201 |
| Related queries | Properties for NDC 9 |
NDC Item 52959009203
| NDC 10 | UNKNOWN |
|---|---|
| NDC Item | 52959009203 |
| Related queries | Properties for NDC 9 |
NDC Item 66267093705
| NDC 10 | UNKNOWN |
|---|---|
| NDC Item | 66267093705 |
| Related queries | Properties for NDC 9 |
NDC Item 00065064705
| NDC 9 | 0065-0647 |
|---|---|
| NDC 10 | 0065-0647-05 |
| NDC Item | 00065064705 |
| Packaging | 5 mL in 1 BOTTLE, PLASTIC (0065-0647-05) |
| FDA SPL set id | 692142 |
| Labeler | Alcon Laboratories, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | NDA |
| Marketing effective time high | 2023-08-31 |
| Marketing effective time low | 1988-09-15 |
| Marketing status | COMPLETED |
| NDA | NDA050592 |
| Related queries | Properties for NDC 9 0065-0647 |
NDC Item 00065064710
| NDC 9 | 0065-0647 |
|---|---|
| NDC 10 | 0065-0647-10 |
| NDC Item | 00065064710 |
| Packaging | 10 mL in 1 BOTTLE, PLASTIC (0065-0647-10) |
| FDA SPL set id | 692142 |
| Labeler | Alcon Laboratories, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | NDA |
| Marketing effective time high | 2023-08-31 |
| Marketing effective time low | 1988-09-15 |
| Marketing status | COMPLETED |
| NDA | NDA050592 |
| Related queries | Properties for NDC 9 0065-0647 |
NDC Item 00065064725
| NDC 9 | 0065-0647 |
|---|---|
| NDC 10 | 0065-0647-25 |
| NDC Item | 00065064725 |
| Packaging | 2.5 mL in 1 BOTTLE, PLASTIC (0065-0647-25) |
| FDA SPL set id | 692142 |
| Labeler | Alcon Laboratories, Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | NDA |
| Marketing effective time high | 2023-08-31 |
| Marketing effective time low | 1988-09-15 |
| Marketing status | COMPLETED |
| NDA | NDA050592 |
| Related queries | Properties for NDC 9 0065-0647 |
NDC Item 00078095325
| NDC 9 | 0078-0953 |
|---|---|
| NDC 10 | 0078-0953-25 |
| NDC Item | 00078095325 |
| Packaging | 5 mL in 1 BOTTLE (0078-0953-25) |
| FDA SPL set id | 706700 |
| Labeler | Novartis Pharmaceuticals Corporation |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | NDA |
| Marketing effective time low | 1988-09-15 |
| Marketing status | ACTIVE |
| NDA | NDA050592 |
| Related queries | Properties for NDC 9 0078-0953 |
NDC Item 00078095326
| NDC 9 | 0078-0953 |
|---|---|
| NDC 10 | 0078-0953-26 |
| NDC Item | 00078095326 |
| Packaging | 10 mL in 1 BOTTLE (0078-0953-26) |
| FDA SPL set id | 706700 |
| Labeler | Novartis Pharmaceuticals Corporation |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | NDA |
| Marketing effective time low | 1988-09-15 |
| Marketing status | ACTIVE |
| NDA | NDA050592 |
| Related queries | Properties for NDC 9 0078-0953 |
NDC Item 00078095340
| NDC 9 | 0078-0953 |
|---|---|
| NDC 10 | 0078-0953-40 |
| NDC Item | 00078095340 |
| Packaging | 2.5 mL in 1 BOTTLE (0078-0953-40) |
| FDA SPL set id | 706700 |
| Labeler | Novartis Pharmaceuticals Corporation |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | NDA |
| Marketing effective time low | 1988-09-15 |
| Marketing status | ACTIVE |
| NDA | NDA050592 |
| Related queries | Properties for NDC 9 0078-0953 |
NDC Item 43063000501
| NDC 10 | UNKNOWN |
|---|---|
| NDC Item | 43063000501 |
| Related queries | Properties for NDC 9 |
NDC Item 52959009200
| NDC 10 | UNKNOWN |
|---|---|
| NDC Item | 52959009200 |
| Related queries | Properties for NDC 9 |
NDC Item 52959009201
| NDC 10 | UNKNOWN |
|---|---|
| NDC Item | 52959009201 |
| Related queries | Properties for NDC 9 |
NDC Item 52959009203
| NDC 10 | UNKNOWN |
|---|---|
| NDC Item | 52959009203 |
| Related queries | Properties for NDC 9 |
NDC Item 66267093705
| NDC 10 | UNKNOWN |
|---|---|
| NDC Item | 66267093705 |
| Related queries | Properties for NDC 9 |