United States · FDA National Drug Code directory
ALBUMINEX
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 64208-2512_85f1cecd-a23d-498f-adfb-0a09feed1994
- Product NDC
- 64208-2512
- Form
- SOLUTION
- Composition / generic term
- Albumin Human
- Labeler
- BPL
- Marketing category
- BLA
- Marketing start / end (source format)
- 20200527
- Source listing expiry
- 20261231
Source-listed ingredients
- ALBUMIN HUMAN — .25 g/mL
These values do not establish equivalence or a dose recommendation.
Packages
- 1 VIAL, GLASS in 1 CARTON (64208-2512-3) / 50 mL in 1 VIAL, GLASS (64208-2512-4) · 64208-2512-3
- 1 VIAL, GLASS in 1 CARTON (64208-2512-7) / 100 mL in 1 VIAL, GLASS (64208-2512-8) · 64208-2512-7
Source and coverage
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Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
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