FDA NDC Directory · JSON-LD · Markdown

ropinirole hydrochloride

NDC 60687-577 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerAmerican Health Packaging
Marketing categoryAbbreviated NDA (generic) · App ANDA078110
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsROPINIROLE HYDROCHLORIDE (.25 mg/1)
Marketing started20210610
Package count1

External sources

Source: openFDA. Public-domain (CC0).