# ALBUMINEX

NDC: 64208-2512
Generic name: Albumin Human
Labeler / Manufacturer: BPL
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Biologic License Application
Dosage form: SOLUTION
Routes: INTRAVENOUS
Marketing started: 20200527

FDA application: BLA125644

## 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:"64208-2512"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=64208-2512
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=167f48d0-8ae5-4f7e-b050-9673dad78acc