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Ropinirole

NDC 64850-252 · HUMAN PRESCRIPTION DRUG · TABLET, EXTENDED RELEASE

Labeler / ManufacturerElite Laboratories, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA217862
Dosage form / routeTABLET, EXTENDED RELEASE · ORAL
Active ingredientsROPINIROLE HYDROCHLORIDE (6 mg/1)
Marketing started20251110
Package count1

External sources

Source: openFDA. Public-domain (CC0).