# ALBUMINEX

NDC: 64208-2510
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: .05 g/mL

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"64208-2510"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=64208-2510
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=8428d373-f4b1-4e3b-bb19-ea89048f7c79