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ROPINIROLE HYDROCHLORIDE

NDC 42291-714 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED, EXTENDED RELEASE

Generic nameropinirole hydrochloride
Labeler / ManufacturerAvKARE
Marketing categoryAbbreviated NDA (generic) · App ANDA090869
Dosage form / routeTABLET, FILM COATED, EXTENDED RELEASE · ORAL
Active ingredientsROPINIROLE HYDROCHLORIDE (4 mg/1)
Marketing started20130913
Package count1

External sources

Source: openFDA. Public-domain (CC0).