FDA NDC Directory · JSON-LD · Markdown

ROPINIROLE

NDC 67046-1489 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerCoupler LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA090429
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsROPINIROLE HYDROCHLORIDE (2 mg/1)
Marketing started20250129
Package count1

External sources

Source: openFDA. Public-domain (CC0).