FDA NDC Directory · JSON-LD · Markdown

ropinirole hydrochloride

NDC 50090-1330 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerA-S Medication Solutions
Marketing categoryAbbreviated NDA (generic) · App ANDA078110
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsROPINIROLE HYDROCHLORIDE (.25 mg/1)
Marketing started20110920
Package count1

External sources

Source: openFDA. Public-domain (CC0).