# AlbuRx

NDC: 44206-251
Generic name: ALBUMIN (HUMAN)
Labeler / Manufacturer: CSL Behring AG
Product type: PLASMA DERIVATIVE
Marketing category: Biologic License Application
Dosage form: SOLUTION
Routes: INTRAVENOUS
Marketing started: 20090106

FDA application: BLA102366

## Active ingredients

- ALBUMIN HUMAN: 12.5 g/50mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"44206-251"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=44206-251