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Eltrombopag Olamine

NDC 69238-1415 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Generic nameEltrombopag
Labeler / ManufacturerAmneal Pharmaceuticals NY LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA212884
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsELTROMBOPAG OLAMINE (50 mg/1)
Marketing started20260115
Package count1

External sources

Source: openFDA. Public-domain (CC0).