FDA NDC Directory · JSON-LD · Markdown

Ropinirole

NDC 69452-362 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerBionpharma Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA079229
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsROPINIROLE HYDROCHLORIDE (5 mg/1)
Marketing started20220915
Package count1

External sources

Source: openFDA. Public-domain (CC0).