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Flexbumin

NDC 0944-0495 · PLASMA DERIVATIVE · INJECTION, SOLUTION

Generic nameAlbumin Human
Labeler / ManufacturerTakeda Pharmaceuticals America, Inc.
Marketing categoryBiologic License Application · App BLA101452
Dosage form / routeINJECTION, SOLUTION · INTRAVENOUS
Active ingredientsALBUMIN HUMAN (.05 g/mL)
Marketing started20140731
Package count1

External sources

Source: openFDA. Public-domain (CC0).