NDC properties for "Timoptic 0.005 MG/MG Ophthalmic Gel" (RxCUI 861422)
About this data
The tables show NDC propoerties for Timoptic 0.005 MG/MG Ophthalmic Gel with the RxCUI 861422
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 0.005 MG/MG Ophthalmic Gel (RxCUI 861422)
| MMSL_CODE | BD3328 |
|---|---|
| NDA | NDA020330 |
| RxCUI | 861422 |
| SPL_SET_ID | a4d03de7-06b7-4cfc-9d1b-616969df209c |
| Prescribable Synonym | Timoptic-XE 0.5 % Ophthalmic Gel Forming Solution |
| RXNAV_STR | Timoptic 0.005 MG/MG Ophthalmic Gel |
| RxNorm Name | timolol 0.005 MG/MG Ophthalmic Gel [Timoptic] |
| RxNorm Synonym | Timoptic 0.005 MG/MG Ophthalmic Gel |
| RxNorm Synonym | Timoptic-XE 0.005 MG/MG Ophthalmic Gel |
| RxNorm Synonym | Timoptic-XE 0.5 % Gel Forming Solution |
| Related queries | Interactions (for RxCUI 861422) |
NDC Properties
NDC Item 24208081605
| NDC 9 | 24208-816 |
|---|---|
| NDC 10 | 24208-816-05 |
| NDC Item | 24208081605 |
| Packaging | 1 BOTTLE, DISPENSING in 1 CARTON (24208-816-05) / 5 mL in 1 BOTTLE, DISPENSING |
| FDA SPL set id | 639370 |
| Labeler | Bausch & Lomb Incorporated |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | NDA |
| Marketing effective time low | 2016-05-31 |
| Marketing status | ACTIVE |
| NDA | NDA020330 |
| Related queries | Properties for NDC 9 24208-816 |
NDC Item 25010081156
| NDC 9 | 25010-811 |
|---|---|
| NDC 10 | 25010-811-56 |
| NDC Item | 25010081156 |
| Packaging | 1 BOTTLE, DISPENSING in 1 CARTON (25010-811-56) / 5 mL in 1 BOTTLE, DISPENSING |
| FDA SPL set id | 282260 |
| Labeler | Bausch Health US, LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | NDA |
| Marketing effective time high | 2018-01-31 |
| Marketing effective time low | 1993-11-14 |
| Marketing status | COMPLETED |
| NDA | NDA020330 |
| Related queries | Properties for NDC 9 25010-811 |
NDC Item 24208081605
| NDC 9 | 24208-816 |
|---|---|
| NDC 10 | 24208-816-05 |
| NDC Item | 24208081605 |
| Packaging | 1 BOTTLE, DISPENSING in 1 CARTON (24208-816-05) / 5 mL in 1 BOTTLE, DISPENSING |
| FDA SPL set id | 639370 |
| Labeler | Bausch & Lomb Incorporated |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | NDA |
| Marketing effective time low | 2016-05-31 |
| Marketing status | ACTIVE |
| NDA | NDA020330 |
| Related queries | Properties for NDC 9 24208-816 |
NDC Item 25010081156
| NDC 9 | 25010-811 |
|---|---|
| NDC 10 | 25010-811-56 |
| NDC Item | 25010081156 |
| Packaging | 1 BOTTLE, DISPENSING in 1 CARTON (25010-811-56) / 5 mL in 1 BOTTLE, DISPENSING |
| FDA SPL set id | 282260 |
| Labeler | Bausch Health US, LLC |
| Label type | HUMAN PRESCRIPTION DRUG |
| Marketing category | NDA |
| Marketing effective time high | 2018-01-31 |
| Marketing effective time low | 1993-11-14 |
| Marketing status | COMPLETED |
| NDA | NDA020330 |
| Related queries | Properties for NDC 9 25010-811 |