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Ropinirole

NDC 10135-676 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Generic nameropinirole
Labeler / ManufacturerMarlex Pharmaceuticals Inc
Marketing categoryAbbreviated NDA (generic) · App ANDA079165
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsROPINIROLE HYDROCHLORIDE (2 mg/1)
Marketing started20190315
Package count1

External sources

Source: openFDA. Public-domain (CC0).