FDA NDC Directory · JSON-LD · Markdown

EPOGEN

NDC 55513-267 · HUMAN PRESCRIPTION DRUG · SOLUTION

Generic nameepoetin alfa
Labeler / ManufacturerAmgen, Inc
Marketing categoryBiologic License Application · App BLA103234
Dosage form / routeSOLUTION · INTRAVENOUS SUBCUTANEOUS
Active ingredientsEPOETIN (3000 [iU]/mL)
Marketing started19900430
Package count2

External sources

Source: openFDA. Public-domain (CC0).