United States · FDA National Drug Code directory
Plasmanate
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
- 13533-613_95aedb83-dbde-418c-bd54-67e580b67c75
- Product NDC
- 13533-613
- Form
- SOLUTION
- Composition / generic term
- Plasma Protein Fraction (Human)
- Labeler
- GRIFOLS USA, LLC
- Marketing category
- BLA
- Marketing start / end (source format)
- 19581002
- Source listing expiry
- 20261231
Source-listed ingredients
- ALBUMIN HUMAN — 2.5 g/50mL
These values do not establish equivalence or a dose recommendation.
Packages
- 1 VIAL in 1 CARTON (13533-613-25) / 250 mL in 1 VIAL (13533-613-26) · 13533-613-25
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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