United States · FDA National Drug Code directory
ALBUTEIN
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
- 68516-5215_c6fbef49-e3bd-4f26-8c83-7a0fb0c3aaf0
- Product NDC
- 68516-5215
- Form
- INJECTION, SOLUTION
- Composition / generic term
- ALBUMIN (HUMAN)
- Labeler
- GRIFOLS USA, LLC
- Marketing category
- BLA
- Marketing start / end (source format)
- 20211108
- Source listing expiry
- 20261231
Source-listed ingredients
- ALBUMIN HUMAN — 10 g/50mL
These values do not establish equivalence or a dose recommendation.
Packages
- 1 BAG in 1 CARTON (68516-5215-7) / 50 mL in 1 BAG (68516-5215-5) · 68516-5215-7
- 1 BAG in 1 CARTON (68516-5215-8) / 100 mL in 1 BAG (68516-5215-6) · 68516-5215-8
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 →