# FLEXBUMIN

NDC: 0944-0493
Generic name: Albumin Human
Labeler / Manufacturer: Takeda Pharmaceuticals America, Inc.
Product type: PLASMA DERIVATIVE
Marketing category: Biologic License Application
Dosage form: SOLUTION
Routes: INTRAVENOUS
Marketing started: 20020809

FDA application: BLA101452

## Active ingredients

- ALBUMIN HUMAN: .25 g/mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0944-0493"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0944-0493