FDA NDC Directory · JSON-LD · Markdown

PROMACTA

NDC 0078-0697 · HUMAN PRESCRIPTION DRUG · POWDER, FOR SUSPENSION

Generic nameeltrombopag olamine
Labeler / ManufacturerNovartis Pharmaceuticals Corporation
Marketing categoryNew Drug Application (innovator) · App NDA207027
Dosage form / routePOWDER, FOR SUSPENSION · ORAL
Active ingredientsELTROMBOPAG OLAMINE (25 mg/1)
Marketing started20180927
Package count1

External sources

Source: openFDA. Public-domain (CC0).