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Pramipexole Dihydrochloride

NDC 46708-612 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerAlembic Pharmaceuticals Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA078894
Dosage form / routeTABLET · ORAL
Active ingredientsPRAMIPEXOLE DIHYDROCHLORIDE (.25 mg/1)
Marketing started20160322
Package count1

External sources

Source: openFDA. Public-domain (CC0).