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KEDBUMIN

NDC 76179-025 · PLASMA DERIVATIVE · INJECTION, SOLUTION

Generic nameAlbumin (Human)
Labeler / ManufacturerKedrion S.p.A
Marketing categoryBiologic License Application · App BLA125384
Dosage form / routeINJECTION, SOLUTION · INTRAVENOUS
Active ingredientsALBUMIN HUMAN (12.5 g/50mL)
Marketing started20110915
Package count2

External sources

Source: openFDA. Public-domain (CC0).