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Ropinirole

NDC 46708-264 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED, EXTENDED RELEASE

Labeler / ManufacturerAlembic Pharmaceuticals Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA202786
Dosage form / routeTABLET, FILM COATED, EXTENDED RELEASE · ORAL
Active ingredientsROPINIROLE HYDROCHLORIDE (6 mg/1)
Marketing started20130314
Package count6

External sources

Source: openFDA. Public-domain (CC0).