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
- 44206-251_4ab3fa50-584a-43fd-a729-472240f3dc3f
- Product NDC
- 44206-251
- Form
- SOLUTION
- Composition / generic term
- ALBUMIN (HUMAN)
- Labeler
- CSL Behring AG
- Marketing category
- BLA
- Marketing start / end (source format)
- 20090106
- Source listing expiry
- 20261231
Source-listed ingredients
- ALBUMIN HUMAN — 12.5 g/50mL
These values do not establish equivalence or a dose recommendation.
Packages
- 1 VIAL, GLASS in 1 CARTON (44206-251-05) / 50 mL in 1 VIAL, GLASS (44206-251-90) · 44206-251-05
- 1 VIAL, GLASS in 1 CARTON (44206-251-10) / 100 mL in 1 VIAL, GLASS (44206-251-91) · 44206-251-10
Source and coverage
Open FDA National Drug Code directory →
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.
Browse United States records →