FDA NDC Directory · JSON-LD · Markdown

ropinirole

NDC 50090-4684 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerA-S Medication Solutions
Marketing categoryAbbreviated NDA (generic) · App ANDA090135
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsROPINIROLE HYDROCHLORIDE (1 mg/1)
Marketing started20100225
Package count2

External sources

Source: openFDA. Public-domain (CC0).