# Albumin (Human)

NDC: 68982-623
Generic name: Albumin Human
Labeler / Manufacturer: Octapharma USA Inc
Product type: PLASMA DERIVATIVE
Marketing category: Biologic License Application
Dosage form: SOLUTION
Routes: INTRAVENOUS
Marketing started: 20061017

FDA application: BLA125154

## Active ingredients

- ALBUMIN HUMAN: 50 g/1000mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"68982-623"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68982-623