FDA NDC Directory · JSON-LD · Markdown

Albuked

NDC 76125-792 · PLASMA DERIVATIVE · SOLUTION

Generic nameAlbumin (Human)
Labeler / ManufacturerKEDRION BIOPHARMA, INC.
Marketing categoryBiologic License Application · App BLA101138
Dosage form / routeSOLUTION · INTRAVENOUS
Active ingredientsALBUMIN HUMAN (5 g/20mL)
Marketing started19421021
Package count3

External sources

Source: openFDA. Public-domain (CC0).