FDA NDC Directory · JSON-LD · Markdown

Albuked

NDC 76125-791 · PLASMA DERIVATIVE · SOLUTION

Generic nameAlbumin (Human)
Labeler / ManufacturerKEDRION BIOPHARMA, INC.
Marketing categoryBiologic License Application · App BLA101138
Dosage form / routeSOLUTION · INTRAVENOUS
Active ingredientsALBUMIN HUMAN (10 g/50mL)
Marketing started19810728
Package count2

External sources

Source: openFDA. Public-domain (CC0).