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Ropinirole

NDC 70518-4318 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerREMEDYREPACK INC.
Marketing categoryAbbreviated NDA (generic) · App ANDA079229
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsROPINIROLE HYDROCHLORIDE (.5 mg/1)
Marketing started20250325
Package count1

External sources

Source: openFDA. Public-domain (CC0).