# ALBUTEIN

NDC: 68516-5216
Generic name: ALBUMIN (HUMAN)
Labeler / Manufacturer: GRIFOLS USA, LLC
Product type: PLASMA DERIVATIVE
Marketing category: Biologic License Application
Dosage form: INJECTION, SOLUTION
Routes: INTRAVENOUS
Marketing started: 20220301

FDA application: BLA102478

## 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:"68516-5216"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68516-5216