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pramipexole dihydrochloride

NDC 64380-749 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerStrides Pharma Science Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA202702
Dosage form / routeTABLET · ORAL
Active ingredientsPRAMIPEXOLE DIHYDROCHLORIDE (.75 mg/1)
Marketing started20210215
Package count1

External sources

Source: openFDA. Public-domain (CC0).