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Ropinirole

NDC 55111-662 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED, EXTENDED RELEASE

Labeler / ManufacturerDr. Reddys Laboratories Limited
Marketing categoryAbbreviated NDA (generic) · App ANDA201576
Dosage form / routeTABLET, FILM COATED, EXTENDED RELEASE · ORAL
Active ingredientsROPINIROLE HYDROCHLORIDE (8 mg/1)
Marketing started20120606
Package count3

External sources

Source: openFDA. Public-domain (CC0).