FDA NDC Directory · JSON-LD · Markdown

Ropinirole

NDC 72189-416 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerDirect_Rx
Marketing categoryAbbreviated NDA (generic) · App ANDA090135
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsROPINIROLE HYDROCHLORIDE (.25 mg/1)
Marketing started20230201
Package count1

External sources

Source: openFDA. Public-domain (CC0).