FDA NDC Directory · JSON-LD · Markdown

Pramipexole Dihydrochloride

NDC 72162-2569 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerBryant Ranch Prepack
Marketing categoryAbbreviated NDA (generic) · App ANDA090865
Dosage form / routeTABLET · ORAL
Active ingredientsPRAMIPEXOLE DIHYDROCHLORIDE (.75 mg/1)
Marketing started20101008
Package count1

External sources

Source: openFDA. Public-domain (CC0).