FDA NDC Directory · JSON-LD · Markdown

ROPINIROLE

NDC 62332-034 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerAlembic Pharmaceuticals Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA090429
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsROPINIROLE HYDROCHLORIDE (3 mg/1)
Marketing started20160129
Package count1

External sources

Source: openFDA. Public-domain (CC0).