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Pramipexole Dihydrochloride

NDC 13668-092 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerTorrent Pharmaceuticals Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA090865
Dosage form / routeTABLET · ORAL
Active ingredientsPRAMIPEXOLE DIHYDROCHLORIDE (.25 mg/1)
Marketing started20101008
Package count4

External sources

Source: openFDA. Public-domain (CC0).