FDA NDC Directory · JSON-LD · Markdown

PROMACTA

NDC 0078-0684 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Generic nameeltrombopag olamine
Labeler / ManufacturerNovartis Pharmaceuticals Corporation
Marketing categoryNew Drug Application (innovator) · App NDA022291
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsELTROMBOPAG OLAMINE (12.5 mg/1)
Marketing started20160822
Package count1

External sources

Source: openFDA. Public-domain (CC0).