NDC properties for "Cosopt PF (dorzolamide 2 % / timolol 0.5 % ) Ophthalmic Solution" (RxCUI 1922784)
About this data
The tables show NDC propoerties for Cosopt PF (dorzolamide 2 % / timolol 0.5 % ) Ophthalmic Solution with the RxCUI 1922784
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 Cosopt PF (dorzolamide 2 % / timolol 0.5 % ) Ophthalmic Solution (RxCUI 1922784)
| MMSL_CODE | BD28812 |
|---|---|
| NDA | NDA202667 |
| RxCUI | 1922784 |
| SPL_SET_ID | 535fc801-8c3f-4974-a120-3eff1d5a5062 |
| SPL_SET_ID | a8d4e2b5-c7bb-48fc-9314-7095cd77617e |
| Prescribable Synonym | COSOPT PF 2 % / 0.5 % Ophthalmic Solution |
| RXNAV_STR | Cosopt PF (dorzolamide 2 % / timolol 0.5 % ) Ophthalmic Solution |
| RxNorm Name | Preservative-Free dorzolamide 20 MG/ML / timolol 5 MG/ML Ophthalmic Solution [Cosopt] |
| RxNorm Synonym | Cosopt PF (dorzolamide 2 % / timolol 0.5 % ) Ophthalmic Solution |
| Related queries | Interactions (for RxCUI 1922784) |
NDC Properties
NDC Item 17478060400
| NDC 9 | 17478-604 |
|---|---|
| NDC 10 | 17478-604-00 |
| NDC Item | 17478060400 |
| Packaging | 0.2 mL in 1 VIAL, SINGLE-USE |
| Packaging | 15 in 1 POUCH |
| FDA SPL set id | 636466 |
| Labeler | Akorn Operating Company LLC (dba Akorn) |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | NDA |
| Marketing effective time low | 2014-05-14 |
| Marketing status | ACTIVE |
| NDA | NDA202667 |
| Related queries | Properties for NDC 9 17478-604 |
NDC Item 17478060401
| NDC 9 | 17478-604 |
|---|---|
| NDC 10 | 17478-604-01 |
| NDC Item | 17478060401 |
| Packaging | 0.2 mL in 1 VIAL, SINGLE-USE |
| Packaging | 15 in 1 POUCH |
| FDA SPL set id | 636466 |
| Labeler | Akorn Operating Company LLC (dba Akorn) |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | NDA |
| Marketing effective time low | 2014-05-14 |
| Marketing status | ACTIVE |
| NDA | NDA202667 |
| Related queries | Properties for NDC 9 17478-604 |
NDC Item 17478060430
| NDC 9 | 17478-604 |
|---|---|
| NDC 10 | 17478-604-30 |
| NDC Item | 17478060430 |
| Packaging | 4 POUCH in 1 CARTON (17478-604-30) / 15 VIAL, SINGLE-USE in 1 POUCH (17478-604-01) / .2 mL in 1 VIAL, SINGLE-USE |
| FDA SPL set id | 636466 |
| Labeler | Akorn Operating Company LLC (dba Akorn) |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | NDA |
| Marketing effective time low | 2014-05-14 |
| Marketing status | ACTIVE |
| NDA | NDA202667 |
| Related queries | Properties for NDC 9 17478-604 |
NDC Item 82584060401
| NDC 9 | 82584-604 |
|---|---|
| NDC 10 | 82584-604-01 |
| NDC Item | 82584060401 |
| Packaging | 0.2 mL in 1 VIAL, SINGLE-DOSE |
| Packaging | 15 in 1 POUCH |
| FDA SPL set id | 761201 |
| Labeler | Thea Pharma Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | NDA |
| Marketing effective time low | 2022-12-10 |
| Marketing status | ACTIVE |
| NDA | NDA202667 |
| Related queries | Properties for NDC 9 82584-604 |
NDC Item 82584060430
| NDC 9 | 82584-604 |
|---|---|
| NDC 10 | 82584-604-30 |
| NDC Item | 82584060430 |
| Packaging | 4 POUCH in 1 CARTON (82584-604-30) / 15 VIAL, SINGLE-DOSE in 1 POUCH (82584-604-01) / .2 mL in 1 VIAL, SINGLE-DOSE |
| FDA SPL set id | 761201 |
| Labeler | Thea Pharma Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | NDA |
| Marketing effective time low | 2022-12-10 |
| Marketing status | ACTIVE |
| NDA | NDA202667 |
| Related queries | Properties for NDC 9 82584-604 |
NDC Item 17478060400
| NDC 9 | 17478-604 |
|---|---|
| NDC 10 | 17478-604-00 |
| NDC Item | 17478060400 |
| Packaging | 0.2 mL in 1 VIAL, SINGLE-USE |
| Packaging | 15 in 1 POUCH |
| FDA SPL set id | 636466 |
| Labeler | Akorn Operating Company LLC (dba Akorn) |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | NDA |
| Marketing effective time low | 2014-05-14 |
| Marketing status | ACTIVE |
| NDA | NDA202667 |
| Related queries | Properties for NDC 9 17478-604 |
NDC Item 17478060401
| NDC 9 | 17478-604 |
|---|---|
| NDC 10 | 17478-604-01 |
| NDC Item | 17478060401 |
| Packaging | 0.2 mL in 1 VIAL, SINGLE-USE |
| Packaging | 15 in 1 POUCH |
| FDA SPL set id | 636466 |
| Labeler | Akorn Operating Company LLC (dba Akorn) |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | NDA |
| Marketing effective time low | 2014-05-14 |
| Marketing status | ACTIVE |
| NDA | NDA202667 |
| Related queries | Properties for NDC 9 17478-604 |
NDC Item 17478060430
| NDC 9 | 17478-604 |
|---|---|
| NDC 10 | 17478-604-30 |
| NDC Item | 17478060430 |
| Packaging | 4 POUCH in 1 CARTON (17478-604-30) / 15 VIAL, SINGLE-USE in 1 POUCH (17478-604-01) / .2 mL in 1 VIAL, SINGLE-USE |
| FDA SPL set id | 636466 |
| Labeler | Akorn Operating Company LLC (dba Akorn) |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | NDA |
| Marketing effective time low | 2014-05-14 |
| Marketing status | ACTIVE |
| NDA | NDA202667 |
| Related queries | Properties for NDC 9 17478-604 |
NDC Item 82584060401
| NDC 9 | 82584-604 |
|---|---|
| NDC 10 | 82584-604-01 |
| NDC Item | 82584060401 |
| Packaging | 0.2 mL in 1 VIAL, SINGLE-DOSE |
| Packaging | 15 in 1 POUCH |
| FDA SPL set id | 761201 |
| Labeler | Thea Pharma Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | NDA |
| Marketing effective time low | 2022-12-10 |
| Marketing status | ACTIVE |
| NDA | NDA202667 |
| Related queries | Properties for NDC 9 82584-604 |
NDC Item 82584060430
| NDC 9 | 82584-604 |
|---|---|
| NDC 10 | 82584-604-30 |
| NDC Item | 82584060430 |
| Packaging | 4 POUCH in 1 CARTON (82584-604-30) / 15 VIAL, SINGLE-DOSE in 1 POUCH (82584-604-01) / .2 mL in 1 VIAL, SINGLE-DOSE |
| FDA SPL set id | 761201 |
| Labeler | Thea Pharma Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | NDA |
| Marketing effective time low | 2022-12-10 |
| Marketing status | ACTIVE |
| NDA | NDA202667 |
| Related queries | Properties for NDC 9 82584-604 |
NDC Item 17478060400
| NDC 9 | 17478-604 |
|---|---|
| NDC 10 | 17478-604-00 |
| NDC Item | 17478060400 |
| Packaging | 0.2 mL in 1 VIAL, SINGLE-USE |
| Packaging | 15 in 1 POUCH |
| FDA SPL set id | 636466 |
| Labeler | Akorn Operating Company LLC (dba Akorn) |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | NDA |
| Marketing effective time low | 2014-05-14 |
| Marketing status | ACTIVE |
| NDA | NDA202667 |
| Related queries | Properties for NDC 9 17478-604 |
NDC Item 17478060401
| NDC 9 | 17478-604 |
|---|---|
| NDC 10 | 17478-604-01 |
| NDC Item | 17478060401 |
| Packaging | 0.2 mL in 1 VIAL, SINGLE-USE |
| Packaging | 15 in 1 POUCH |
| FDA SPL set id | 636466 |
| Labeler | Akorn Operating Company LLC (dba Akorn) |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | NDA |
| Marketing effective time low | 2014-05-14 |
| Marketing status | ACTIVE |
| NDA | NDA202667 |
| Related queries | Properties for NDC 9 17478-604 |
NDC Item 17478060430
| NDC 9 | 17478-604 |
|---|---|
| NDC 10 | 17478-604-30 |
| NDC Item | 17478060430 |
| Packaging | 4 POUCH in 1 CARTON (17478-604-30) / 15 VIAL, SINGLE-USE in 1 POUCH (17478-604-01) / .2 mL in 1 VIAL, SINGLE-USE |
| FDA SPL set id | 636466 |
| Labeler | Akorn Operating Company LLC (dba Akorn) |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | NDA |
| Marketing effective time low | 2014-05-14 |
| Marketing status | ACTIVE |
| NDA | NDA202667 |
| Related queries | Properties for NDC 9 17478-604 |
NDC Item 82584060401
| NDC 9 | 82584-604 |
|---|---|
| NDC 10 | 82584-604-01 |
| NDC Item | 82584060401 |
| Packaging | 0.2 mL in 1 VIAL, SINGLE-DOSE |
| Packaging | 15 in 1 POUCH |
| FDA SPL set id | 761201 |
| Labeler | Thea Pharma Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | NDA |
| Marketing effective time low | 2022-12-10 |
| Marketing status | ACTIVE |
| NDA | NDA202667 |
| Related queries | Properties for NDC 9 82584-604 |
NDC Item 82584060430
| NDC 9 | 82584-604 |
|---|---|
| NDC 10 | 82584-604-30 |
| NDC Item | 82584060430 |
| Packaging | 4 POUCH in 1 CARTON (82584-604-30) / 15 VIAL, SINGLE-DOSE in 1 POUCH (82584-604-01) / .2 mL in 1 VIAL, SINGLE-DOSE |
| FDA SPL set id | 761201 |
| Labeler | Thea Pharma Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | NDA |
| Marketing effective time low | 2022-12-10 |
| Marketing status | ACTIVE |
| NDA | NDA202667 |
| Related queries | Properties for NDC 9 82584-604 |
NDC Item 17478060400
| NDC 9 | 17478-604 |
|---|---|
| NDC 10 | 17478-604-00 |
| NDC Item | 17478060400 |
| Packaging | 0.2 mL in 1 VIAL, SINGLE-USE |
| Packaging | 15 in 1 POUCH |
| FDA SPL set id | 636466 |
| Labeler | Akorn Operating Company LLC (dba Akorn) |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | NDA |
| Marketing effective time low | 2014-05-14 |
| Marketing status | ACTIVE |
| NDA | NDA202667 |
| Related queries | Properties for NDC 9 17478-604 |
NDC Item 17478060401
| NDC 9 | 17478-604 |
|---|---|
| NDC 10 | 17478-604-01 |
| NDC Item | 17478060401 |
| Packaging | 0.2 mL in 1 VIAL, SINGLE-USE |
| Packaging | 15 in 1 POUCH |
| FDA SPL set id | 636466 |
| Labeler | Akorn Operating Company LLC (dba Akorn) |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | NDA |
| Marketing effective time low | 2014-05-14 |
| Marketing status | ACTIVE |
| NDA | NDA202667 |
| Related queries | Properties for NDC 9 17478-604 |
NDC Item 17478060430
| NDC 9 | 17478-604 |
|---|---|
| NDC 10 | 17478-604-30 |
| NDC Item | 17478060430 |
| Packaging | 4 POUCH in 1 CARTON (17478-604-30) / 15 VIAL, SINGLE-USE in 1 POUCH (17478-604-01) / .2 mL in 1 VIAL, SINGLE-USE |
| FDA SPL set id | 636466 |
| Labeler | Akorn Operating Company LLC (dba Akorn) |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | NDA |
| Marketing effective time low | 2014-05-14 |
| Marketing status | ACTIVE |
| NDA | NDA202667 |
| Related queries | Properties for NDC 9 17478-604 |
NDC Item 82584060401
| NDC 9 | 82584-604 |
|---|---|
| NDC 10 | 82584-604-01 |
| NDC Item | 82584060401 |
| Packaging | 0.2 mL in 1 VIAL, SINGLE-DOSE |
| Packaging | 15 in 1 POUCH |
| FDA SPL set id | 761201 |
| Labeler | Thea Pharma Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | NDA |
| Marketing effective time low | 2022-12-10 |
| Marketing status | ACTIVE |
| NDA | NDA202667 |
| Related queries | Properties for NDC 9 82584-604 |
NDC Item 82584060430
| NDC 9 | 82584-604 |
|---|---|
| NDC 10 | 82584-604-30 |
| NDC Item | 82584060430 |
| Packaging | 4 POUCH in 1 CARTON (82584-604-30) / 15 VIAL, SINGLE-DOSE in 1 POUCH (82584-604-01) / .2 mL in 1 VIAL, SINGLE-DOSE |
| FDA SPL set id | 761201 |
| Labeler | Thea Pharma Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | NDA |
| Marketing effective time low | 2022-12-10 |
| Marketing status | ACTIVE |
| NDA | NDA202667 |
| Related queries | Properties for NDC 9 82584-604 |
NDC Item 17478060400
| NDC 9 | 17478-604 |
|---|---|
| NDC 10 | 17478-604-00 |
| NDC Item | 17478060400 |
| Packaging | 0.2 mL in 1 VIAL, SINGLE-USE |
| Packaging | 15 in 1 POUCH |
| FDA SPL set id | 636466 |
| Labeler | Akorn Operating Company LLC (dba Akorn) |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | NDA |
| Marketing effective time low | 2014-05-14 |
| Marketing status | ACTIVE |
| NDA | NDA202667 |
| Related queries | Properties for NDC 9 17478-604 |
NDC Item 17478060401
| NDC 9 | 17478-604 |
|---|---|
| NDC 10 | 17478-604-01 |
| NDC Item | 17478060401 |
| Packaging | 0.2 mL in 1 VIAL, SINGLE-USE |
| Packaging | 15 in 1 POUCH |
| FDA SPL set id | 636466 |
| Labeler | Akorn Operating Company LLC (dba Akorn) |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | NDA |
| Marketing effective time low | 2014-05-14 |
| Marketing status | ACTIVE |
| NDA | NDA202667 |
| Related queries | Properties for NDC 9 17478-604 |
NDC Item 17478060430
| NDC 9 | 17478-604 |
|---|---|
| NDC 10 | 17478-604-30 |
| NDC Item | 17478060430 |
| Packaging | 4 POUCH in 1 CARTON (17478-604-30) / 15 VIAL, SINGLE-USE in 1 POUCH (17478-604-01) / .2 mL in 1 VIAL, SINGLE-USE |
| FDA SPL set id | 636466 |
| Labeler | Akorn Operating Company LLC (dba Akorn) |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | NDA |
| Marketing effective time low | 2014-05-14 |
| Marketing status | ACTIVE |
| NDA | NDA202667 |
| Related queries | Properties for NDC 9 17478-604 |
NDC Item 82584060401
| NDC 9 | 82584-604 |
|---|---|
| NDC 10 | 82584-604-01 |
| NDC Item | 82584060401 |
| Packaging | 0.2 mL in 1 VIAL, SINGLE-DOSE |
| Packaging | 15 in 1 POUCH |
| FDA SPL set id | 761201 |
| Labeler | Thea Pharma Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | NDA |
| Marketing effective time low | 2022-12-10 |
| Marketing status | ACTIVE |
| NDA | NDA202667 |
| Related queries | Properties for NDC 9 82584-604 |
NDC Item 82584060430
| NDC 9 | 82584-604 |
|---|---|
| NDC 10 | 82584-604-30 |
| NDC Item | 82584060430 |
| Packaging | 4 POUCH in 1 CARTON (82584-604-30) / 15 VIAL, SINGLE-DOSE in 1 POUCH (82584-604-01) / .2 mL in 1 VIAL, SINGLE-DOSE |
| FDA SPL set id | 761201 |
| Labeler | Thea Pharma Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | NDA |
| Marketing effective time low | 2022-12-10 |
| Marketing status | ACTIVE |
| NDA | NDA202667 |
| Related queries | Properties for NDC 9 82584-604 |