FDA NDC Directory · JSON-LD · Markdown

ropinirole

NDC 16729-233 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerAccord Healthcare Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA204022
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsROPINIROLE HYDROCHLORIDE (.5 mg/1)
Marketing started20181017
Package count1

External sources

Source: openFDA. Public-domain (CC0).