FDA NDC Directory · JSON-LD · Markdown

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NDC 0173-0897 · HUMAN PRESCRIPTION DRUG · TABLET, FILM COATED

Generic namedaprodustat
Labeler / ManufacturerGlaxoSmithKline LLC
Marketing categoryNew Drug Application (innovator) · App NDA216951
Dosage form / routeTABLET, FILM COATED · ORAL
Active ingredientsDAPRODUSTAT (1 mg/1)
Marketing started20230201
Marketing ended20270131
Package count1

External sources

Source: openFDA. Public-domain (CC0).