United States · FDA National Drug Code directory
ALBURX
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
- 44206-310_76269907-bb6e-4724-bc94-88cb77674107
- Product NDC
- 44206-310
- Form
- SOLUTION
- Composition / generic term
- ALBUMIN (HUMAN)
- Labeler
- CSL Behring AG
- Marketing category
- BLA
- Marketing start / end (source format)
- 20090106
- Source listing expiry
- 20271231
Source-listed ingredients
- ALBUMIN HUMAN — 12.5 g/250mL
These values do not establish equivalence or a dose recommendation.
Packages
- 1 VIAL, GLASS in 1 CARTON (44206-310-25) / 250 mL in 1 VIAL, GLASS (44206-310-90) · 44206-310-25
- 1 VIAL, GLASS in 1 CARTON (44206-310-50) / 500 mL in 1 VIAL, GLASS (44206-310-91) · 44206-310-50
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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