FDA NDC Directory · JSON-LD · Markdown

Pramipexole Dihydrochloride

NDC 57237-182 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerRising Pharma Holdings, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA202633
Dosage form / routeTABLET · ORAL
Active ingredientsPRAMIPEXOLE DIHYDROCHLORIDE (.5 mg/1)
Marketing started20121026
Package count2

External sources

Source: openFDA. Public-domain (CC0).