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Eltrombopag

NDC 70377-186 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Generic nameeltrombopag olamine
Labeler / ManufacturerBiocon Pharma Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA220660
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsELTROMBOPAG OLAMINE (75 mg/1)
Marketing started20260909
Package count2

External sources

Source: openFDA. Public-domain (CC0).