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Pramipexole Dihydrochloride

NDC 33342-212 · HUMAN PRESCRIPTION DRUG · TABLET, EXTENDED RELEASE

Labeler / ManufacturerMacleods Pharmaceuticals Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA206156
Dosage form / routeTABLET, EXTENDED RELEASE · ORAL
Active ingredientsPRAMIPEXOLE DIHYDROCHLORIDE (3 mg/1)
Marketing started20200824
Package count2

External sources

Source: openFDA. Public-domain (CC0).