# Plasbumin

NDC: 13533-690
Generic name: Albumin (Human)
Labeler / Manufacturer: GRIFOLS USA, LLC
Product type: PLASMA DERIVATIVE
Marketing category: Biologic License Application
Dosage form: SOLUTION
Routes: INTRAVENOUS
Marketing started: 19940926

FDA application: BLA101138

## Active ingredients

- ALBUMIN HUMAN: 2.5 g/50mL

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"13533-690"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=13533-690