Data / Drug companies / Human Serum Albumin
Human Serum Albumin drugs: 3 drugs from 10 companies in the FDA NDC directory
Human Serum Albumin is an FDA established pharmacologic class. The FDA National Drug Code Directory lists 26 products in this class from 10 companies, covering 3 drugs by generic name. The main marketing category is biologics (BLA), and the newest product started marketing on November 15, 2023.
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- 10Companies
- 26Products
- 3Drugs by generic name
Drugs in the Human Serum Albumin class
Ranked by number of companies that list the drug.
| Drug | Products here | Companies listing it |
|---|---|---|
| Albumin (human) | 17 | 6 |
| Albumin human | 7 | 3 |
| Plasma protein fraction (human) | 1 | 1 |
Companies with the most products in this class
| Company | Products | Main dosage forms | Main marketing category | Newest product started |
|---|---|---|---|---|
| Grifols USA, LLC | 7 | injection, solution | Biologics (BLA) | November 15, 2023 |
| Grifols USA, LLC | 4 | solution | Biologics (BLA) | September 26, 1994 |
| Kedrion Biopharma, Inc. | 3 | solution | Biologics (BLA) | July 28, 1981 |
| Octapharma USA Inc | 3 | solution | Biologics (BLA) | October 17, 2006 |
| Bio Products Laboratory Ltd | 2 | solution | Biologics (BLA) | May 27, 2020 |
| CSL Behring AG | 2 | solution | Biologics (BLA) | January 6, 2009 |
| Takeda Pharmaceuticals America, Inc. | 2 | solution; injection, solution | Biologics (BLA) | July 31, 2014 |
| Grifols USA, LLC | 1 | solution | Biologics (BLA) | February 17, 1995 |
| Kedrion S.p.A | 1 | injection, solution | Biologics (BLA) | September 15, 2011 |
| Professional Complementary Health Formulas | 1 | liquid | Unapproved homeopathic products | August 15, 1984 |
Dosage forms
| Dosage form | Products | Share |
|---|---|---|
| Solution | 16 | 61.5% |
| Injection, solution | 9 | 34.6% |
| Liquid | 1 | 3.8% |
Updated November 6, 2026. Read from US Food and Drug Administration, National Drug Code Directory (openFDA). CC0 1.0 public domain dedication (openFDA). Counts are products in the FDA National Drug Code Directory on November 6, 2026: 138,262 products in commercial distribution, meaning without a marketing end date in the past. A company is a labeler code; one company can hold several codes, and the directory carries no address. Inclusion in the directory is not FDA approval, and the marketing category says under which kind of application or rule a product is sold. This page uses openFDA data and is not endorsed or certified by FDA. Free to reuse with credit to SpecStream under CC BY 4.0. Spot a wrong value? Write to [email protected] with the link to this page.