FDA NDC Directory · JSON-LD · Markdown

ROPINIROLE

NDC 72189-222 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerDIRECT RX
Marketing categoryAbbreviated NDA (generic) · App ANDA204022
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsROPINIROLE HYDROCHLORIDE (1 mg/1)
Marketing started20210520
Package count2

External sources

Source: openFDA. Public-domain (CC0).