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NDC 55513-032 · HUMAN PRESCRIPTION DRUG · INJECTION, SOLUTION

Generic namedarbepoetin alfa
Labeler / ManufacturerAmgen, Inc
Marketing categoryBiologic License Application · App BLA103951
Dosage form / routeINJECTION, SOLUTION · INTRAVENOUS SUBCUTANEOUS
Active ingredientsDARBEPOETIN ALFA (500 ug/mL)
Marketing started20060607
Package count1

External sources

Source: openFDA. Public-domain (CC0).