NDC properties for "Timoptic PF 0.25 % Ophthalmic Solution" (RxCUI 1922877)
About this data
The tables show NDC propoerties for Timoptic PF 0.25 % Ophthalmic Solution with the RxCUI 1922877
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 Timoptic PF 0.25 % Ophthalmic Solution (RxCUI 1922877)
| MMSL_CODE | BD33264 |
|---|---|
| MMSL_CODE | BD3329 |
| NDA | NDA019463 |
| RxCUI | 1922877 |
| SPL_SET_ID | c1293d51-b633-486c-8e13-fcf60063faeb |
| SPL_SET_ID | d130f0ec-c3b5-4bc3-8f4a-68fd6c3ec0cf |
| Prescribable Synonym | Timoptic PF 0.25 % Ophthalmic Solution |
| RXNAV_STR | Timoptic PF 0.25 % Ophthalmic Solution |
| RxNorm Name | Preservative-Free timolol 2.5 MG/ML Ophthalmic Solution [Timoptic] |
| RxNorm Synonym | Timoptic PF 0.25 % Ophthalmic Solution |
| RxNorm Synonym | Timoptic PF 2.5 MG/ML Ophthalmic Solution |
| Related queries | Interactions (for RxCUI 1922877) |
NDC Properties
NDC Item 00187149825
| NDC 9 | 0187-1498 |
|---|---|
| NDC 10 | 0187-1498-25 |
| NDC Item | 00187149825 |
| Packaging | 4 POUCH in 1 CARTON (0187-1498-25) / 15 CONTAINER in 1 POUCH / .3 mL in 1 CONTAINER |
| FDA SPL set id | 465334 |
| Labeler | Bausch Health US LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | NDA |
| Marketing effective time low | 1986-11-05 |
| Marketing status | ACTIVE |
| NDA | NDA019463 |
| Related queries | Properties for NDC 9 0187-1498 |
NDC Item 24208049834
| NDC 9 | 24208-498 |
|---|---|
| NDC 10 | 24208-498-34 |
| NDC Item | 24208049834 |
| Packaging | 6 POUCH in 1 CARTON (24208-498-34) / 10 CONTAINER in 1 POUCH / .3 mL in 1 CONTAINER |
| FDA SPL set id | 622920 |
| Labeler | Bausch & Lomb Incorporated |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | NDA |
| Marketing effective time low | 2022-02-17 |
| Marketing status | ACTIVE |
| NDA | NDA019463 |
| Related queries | Properties for NDC 9 24208-498 |
NDC Item 00187149825
| NDC 9 | 0187-1498 |
|---|---|
| NDC 10 | 0187-1498-25 |
| NDC Item | 00187149825 |
| Packaging | 4 POUCH in 1 CARTON (0187-1498-25) / 15 CONTAINER in 1 POUCH / .3 mL in 1 CONTAINER |
| FDA SPL set id | 465334 |
| Labeler | Bausch Health US LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | NDA |
| Marketing effective time low | 1986-11-05 |
| Marketing status | ACTIVE |
| NDA | NDA019463 |
| Related queries | Properties for NDC 9 0187-1498 |
NDC Item 24208049834
| NDC 9 | 24208-498 |
|---|---|
| NDC 10 | 24208-498-34 |
| NDC Item | 24208049834 |
| Packaging | 6 POUCH in 1 CARTON (24208-498-34) / 10 CONTAINER in 1 POUCH / .3 mL in 1 CONTAINER |
| FDA SPL set id | 622920 |
| Labeler | Bausch & Lomb Incorporated |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | NDA |
| Marketing effective time low | 2022-02-17 |
| Marketing status | ACTIVE |
| NDA | NDA019463 |
| Related queries | Properties for NDC 9 24208-498 |