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Pramipexole Dihydrochloride

NDC 60429-088 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerGolden State Medical Supply, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA203855
Dosage form / routeTABLET · ORAL
Active ingredientsPRAMIPEXOLE DIHYDROCHLORIDE (.75 mg/1)
Marketing started20141028
Package count1

External sources

Source: openFDA. Public-domain (CC0).