FDA NDC Directory · JSON-LD · Markdown

Brimonidine Tartrate

NDC 71921-185 · HUMAN PRESCRIPTION DRUG · SOLUTION/ DROPS

Labeler / ManufacturerFlorida Pharmaceutical Products, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA091691
Dosage form / routeSOLUTION/ DROPS · OPHTHALMIC
Active ingredientsBRIMONIDINE TARTRATE (2 mg/mg)
Marketing started20220115
Package count3

External sources

Source: openFDA. Public-domain (CC0).