FDA NDC Directory · JSON-LD · Markdown

ROPINIROLE

NDC 0904-6373 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Labeler / ManufacturerMajor Pharmaceuticals
Marketing categoryAbbreviated NDA (generic) · App ANDA090429
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsROPINIROLE HYDROCHLORIDE (.25 mg/1)
Marketing started20141001
Package count1

External sources

Source: openFDA. Public-domain (CC0).