FDA NDC Directory · JSON-LD · Markdown

ropinirole

NDC 68788-4138 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerPreferred Pharmaceuticals Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA090135
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsROPINIROLE HYDROCHLORIDE (2 mg/1)
Marketing started20260706
Package count1

External sources

Source: openFDA. Public-domain (CC0).