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Pramipexole Dihydrochloride

NDC 60687-592 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerAmerican Health Packaging
Marketing categoryAbbreviated NDA (generic) · App ANDA090865
Dosage form / routeTABLET · ORAL
Active ingredientsPRAMIPEXOLE DIHYDROCHLORIDE (1 mg/1)
Marketing started20200810
Package count1

External sources

Source: openFDA. Public-domain (CC0).