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brimonidine tartrate

NDC 42571-462 · HUMAN PRESCRIPTION DRUG · SOLUTION/ DROPS

Labeler / ManufacturerMicro Labs Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA218558
Dosage form / routeSOLUTION/ DROPS · OPHTHALMIC
Active ingredientsBRIMONIDINE TARTRATE (1 mg/mL)
Marketing started20260701
Package count2

External sources

Source: openFDA. Public-domain (CC0).