NDC properties for "Timoptic 0.25 % Ophthalmic Solution" (RxCUI 1923429)
About this data
The tables show NDC propoerties for Timoptic 0.25 % Ophthalmic Solution with the RxCUI 1923429
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 0.25 % Ophthalmic Solution (RxCUI 1923429)
| MMSL_CODE | BD3329 |
|---|---|
| NDA | NDA018086 |
| RxCUI | 1923429 |
| SPL_SET_ID | 45ac65b3-19f7-4f33-aebf-cadd3daa4bf1 |
| Prescribable Synonym | TIMOPTIC 0.25 % Ophthalmic Solution |
| RXNAV_STR | Timoptic 0.25 % Ophthalmic Solution |
| RxNorm Name | timolol 2.5 MG/ML Ophthalmic Solution [Timoptic] |
| RxNorm Synonym | Timoptic 0.25 % Ophthalmic Solution |
| RxNorm Synonym | Timoptic 2.5 MG (timolol maleate 3.4 MG) per ML Ophthalmic Solution |
| Related queries | Interactions (for RxCUI 1923429) |
NDC Properties
NDC Item 24208081205
| NDC 9 | 24208-812 |
|---|---|
| NDC 10 | 24208-812-05 |
| NDC Item | 24208081205 |
| Packaging | 1 BOTTLE, DISPENSING in 1 CARTON (24208-812-05) / 5 mL in 1 BOTTLE, DISPENSING |
| FDA SPL set id | 656359 |
| Labeler | Bausch & Lomb Incorporated |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | NDA |
| Marketing effective time low | 2016-12-30 |
| Marketing status | ACTIVE |
| NDA | NDA018086 |
| Related queries | Properties for NDC 9 24208-812 |
NDC Item 25010081256
| NDC 9 | 25010-812 |
|---|---|
| NDC 10 | 25010-812-56 |
| NDC Item | 25010081256 |
| Packaging | 1 BOTTLE, DISPENSING in 1 CARTON (25010-812-56) / 5 mL in 1 BOTTLE, DISPENSING |
| FDA SPL set id | 105872 |
| Labeler | Bausch Health US, LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | NDA |
| Marketing effective time low | 1978-08-17 |
| Marketing status | COMPLETED |
| NDA | NDA018086 |
| Related queries | Properties for NDC 9 25010-812 |
NDC Item 24208081205
| NDC 9 | 24208-812 |
|---|---|
| NDC 10 | 24208-812-05 |
| NDC Item | 24208081205 |
| Packaging | 1 BOTTLE, DISPENSING in 1 CARTON (24208-812-05) / 5 mL in 1 BOTTLE, DISPENSING |
| FDA SPL set id | 656359 |
| Labeler | Bausch & Lomb Incorporated |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | NDA |
| Marketing effective time low | 2016-12-30 |
| Marketing status | ACTIVE |
| NDA | NDA018086 |
| Related queries | Properties for NDC 9 24208-812 |
NDC Item 25010081256
| NDC 9 | 25010-812 |
|---|---|
| NDC 10 | 25010-812-56 |
| NDC Item | 25010081256 |
| Packaging | 1 BOTTLE, DISPENSING in 1 CARTON (25010-812-56) / 5 mL in 1 BOTTLE, DISPENSING |
| FDA SPL set id | 105872 |
| Labeler | Bausch Health US, LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | NDA |
| Marketing effective time low | 1978-08-17 |
| Marketing status | COMPLETED |
| NDA | NDA018086 |
| Related queries | Properties for NDC 9 25010-812 |