FDA NDC Directory · JSON-LD · Markdown

Ropinirole

NDC 72189-494 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerDirect_Rx
Marketing categoryAbbreviated NDA (generic) · App ANDA079229
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsROPINIROLE HYDROCHLORIDE (1 mg/1)
Marketing started20230622
Package count1

External sources

Source: openFDA. Public-domain (CC0).