NDC properties for "Cosopt (dorzolamide 20 MG / timolol 5 MG) per ML Ophthalmic Solution" (RxCUI 1923433)
About this data
The tables show NDC propoerties for Cosopt (dorzolamide 20 MG / timolol 5 MG) per ML Ophthalmic Solution with the RxCUI 1923433
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 (dorzolamide 20 MG / timolol 5 MG) per ML Ophthalmic Solution (RxCUI 1923433)
| MMSL_CODE | BD6611 |
|---|---|
| NDA | NDA020869 |
| RxCUI | 1923433 |
| SPL_SET_ID | 23bdf1c1-3134-4ad1-8e7c-bc655156bdc6 |
| SPL_SET_ID | 44e3bbcd-01d4-4dba-be22-308dffecf236 |
| SPL_SET_ID | b7aa1986-1c24-4733-96b3-e6d8e1d44558 |
| Prescribable Synonym | COSOPT 2 % / 0.5 % Ophthalmic Solution |
| RXNAV_STR | Cosopt 2 % / 0.5 % Ophthalmic Solution |
| RxNorm Name | dorzolamide 20 MG/ML / timolol 5 MG/ML Ophthalmic Solution [Cosopt] |
| RxNorm Synonym | Cosopt (dorzolamide 20 MG / timolol 5 MG) per ML Ophthalmic Solution |
| RxNorm Synonym | Cosopt 2 % / 0.5 % Ophthalmic Solution |
| Related queries | Interactions (for RxCUI 1923433) |
NDC Properties
NDC Item 17478060510
| NDC 9 | 17478-605 |
|---|---|
| NDC 10 | 17478-605-10 |
| NDC Item | 17478060510 |
| Packaging | 1 BOTTLE, DROPPER in 1 CARTON (17478-605-10) / 10 mL in 1 BOTTLE, DROPPER |
| FDA SPL set id | 674330 |
| Labeler | Akorn Operating Company LLC (dba Akorn) |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | NDA |
| Marketing effective time low | 2014-04-30 |
| Marketing status | ACTIVE |
| NDA | NDA020869 |
| Related queries | Properties for NDC 9 17478-605 |
NDC Item 35356010001
| NDC 10 | UNKNOWN |
|---|---|
| NDC Item | 35356010001 |
| Related queries | Properties for NDC 9 |
NDC Item 82584060510
| NDC 9 | 82584-605 |
|---|---|
| NDC 10 | 82584-605-10 |
| NDC Item | 82584060510 |
| Packaging | 1 BOTTLE, DROPPER in 1 CARTON (82584-605-10) / 10 mL in 1 BOTTLE, DROPPER |
| FDA SPL set id | 783291 |
| Labeler | Thea Pharma Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | NDA |
| Marketing effective time low | 2022-11-10 |
| Marketing status | ACTIVE |
| NDA | NDA020869 |
| Related queries | Properties for NDC 9 82584-605 |
NDC Item 17478060510
| NDC 9 | 17478-605 |
|---|---|
| NDC 10 | 17478-605-10 |
| NDC Item | 17478060510 |
| Packaging | 1 BOTTLE, DROPPER in 1 CARTON (17478-605-10) / 10 mL in 1 BOTTLE, DROPPER |
| FDA SPL set id | 674330 |
| Labeler | Akorn Operating Company LLC (dba Akorn) |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | NDA |
| Marketing effective time low | 2014-04-30 |
| Marketing status | ACTIVE |
| NDA | NDA020869 |
| Related queries | Properties for NDC 9 17478-605 |
NDC Item 35356010001
| NDC 10 | UNKNOWN |
|---|---|
| NDC Item | 35356010001 |
| Related queries | Properties for NDC 9 |
NDC Item 82584060510
| NDC 9 | 82584-605 |
|---|---|
| NDC 10 | 82584-605-10 |
| NDC Item | 82584060510 |
| Packaging | 1 BOTTLE, DROPPER in 1 CARTON (82584-605-10) / 10 mL in 1 BOTTLE, DROPPER |
| FDA SPL set id | 783291 |
| Labeler | Thea Pharma Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | NDA |
| Marketing effective time low | 2022-11-10 |
| Marketing status | ACTIVE |
| NDA | NDA020869 |
| Related queries | Properties for NDC 9 82584-605 |
NDC Item 17478060510
| NDC 9 | 17478-605 |
|---|---|
| NDC 10 | 17478-605-10 |
| NDC Item | 17478060510 |
| Packaging | 1 BOTTLE, DROPPER in 1 CARTON (17478-605-10) / 10 mL in 1 BOTTLE, DROPPER |
| FDA SPL set id | 674330 |
| Labeler | Akorn Operating Company LLC (dba Akorn) |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | NDA |
| Marketing effective time low | 2014-04-30 |
| Marketing status | ACTIVE |
| NDA | NDA020869 |
| Related queries | Properties for NDC 9 17478-605 |
NDC Item 35356010001
| NDC 10 | UNKNOWN |
|---|---|
| NDC Item | 35356010001 |
| Related queries | Properties for NDC 9 |
NDC Item 82584060510
| NDC 9 | 82584-605 |
|---|---|
| NDC 10 | 82584-605-10 |
| NDC Item | 82584060510 |
| Packaging | 1 BOTTLE, DROPPER in 1 CARTON (82584-605-10) / 10 mL in 1 BOTTLE, DROPPER |
| FDA SPL set id | 783291 |
| Labeler | Thea Pharma Inc. |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | NDA |
| Marketing effective time low | 2022-11-10 |
| Marketing status | ACTIVE |
| NDA | NDA020869 |
| Related queries | Properties for NDC 9 82584-605 |