Brimonidine
- Product NDC
- 50090-1046
- 11-digit product format
- 500901046
- Labeler code
- 50090
- Product ID
- 50090-1046_47e74411-fd63-40a8-a821-d54ce163ce06
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Brimonidine Tartrate
- Dosage form
- SOLUTION/ DROPS
- Route
- OPHTHALMIC
- Labeler
- A-S Medication Solutions
- Application
- ANDA076439
- Marketing category
- ANDA
- Marketing start
- 2006-09-07
- Marketing end
- 0000-00-00
- Substance
- BRIMONIDINE TARTRATE
- Active strength
- 2 mg/mL
- Pharmacologic classes
- Adrenergic alpha-Agonists [MoA],alpha-Adrenergic Agonist [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2022-12-31
- Current FDA listing
- Historical FDA.report record
FDA-Initiated Inactive NDC Indexing#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 50090-1046-0 | 50090104600 | 1 BOTTLE, DROPPER in 1 CARTON (50090-1046-0) > 5 mL in 1 BOTTLE, DROPPER | 2014-11-28 | 0000-00-00 | No | No | Current |