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Pramipexole dihydrochloride

NDC 33342-034 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerMacleods Pharmaceuticals Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA202164
Dosage form / routeTABLET · ORAL
Active ingredientsPRAMIPEXOLE DIHYDROCHLORIDE (1 mg/1)
Marketing started20120921
Package count4

External sources

Source: openFDA. Public-domain (CC0).