Data / Drug companies / Wyeth BioPharma Division of Wyeth Pharmaceuticals LLC
Wyeth BioPharma Division of Wyeth Pharmaceuticals LLC: 17 products in the FDA NDC directory, labeler code 58394
Updated November 6, 2026. Source: US Food and Drug Administration, National Drug Code Directory (openFDA).
Wyeth BioPharma Division of Wyeth Pharmaceuticals LLC (labeler code 58394) lists 17 products in the FDA National Drug Code Directory, covering 2 finished drugs by generic name. By type: 14 plasma derivatives, 2 drugs for further processing. Its main marketing category is biologics (BLA). The newest product started marketing on September 19, 2019.
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- Labeler code
- 58394
- Products in commercial distribution
- 17
- Packages
- 17
- Finished drugs by generic name
- 2
- Prescription products
- 0
- Over the counter products
- 0
- Started marketing in the last 12 months
- 0
- Earliest marketing start
- February 1, 1997
- openFDA record search
- api.fda.gov
Products by marketing category
Share of the company's products in commercial distribution.
| Marketing category | Products | Share |
|---|---|---|
| Biologics (BLA) | 14 | 82.4% |
| Drugs for further processing | 2 | 11.8% |
| Bulk ingredients | 1 | 5.9% |
Products by type
| Type | Products | Share |
|---|---|---|
| Plasma derivatives | 14 | 82.4% |
| Drugs for further processing | 2 | 11.8% |
| Bulk ingredients | 1 | 5.9% |
Drugs it lists
Finished drugs by generic name, with how many companies list each.
| Drug | Products | Companies listing it |
|---|---|---|
| Antihemophilic factor (recombinant) | 9 | 4 |
| Coagulation factor ix (recombinant) | 5 | 3 |
Dosage forms
| Dosage form | Products | Share |
|---|---|---|
| Kit | 14 | 82.4% |
| Liquid | 3 | 17.6% |
Newest products
By marketing start date.
| Product | Product NDC | Dosage form | Marketing category | Marketing start |
|---|---|---|---|---|
| Bevacizumab | 58394-095 | Liquid | Drugs for further processing | September 19, 2019 |
| Adalimumab | 58394-051 | Liquid | Drugs for further processing | September 19, 2019 |
| BeneFIX | 58394-637 | Kit | Biologics (BLA) | February 1, 2012 |
| Xyntha | 58394-023 | Kit | Biologics (BLA) | December 1, 2011 |
| Xyntha | 58394-022 | Kit | Biologics (BLA) | December 1, 2011 |
| Xyntha | 58394-025 | Kit | Biologics (BLA) | August 1, 2011 |
| Xyntha | 58394-024 | Kit | Biologics (BLA) | August 1, 2011 |
| Xyntha | 58394-016 | Kit | Biologics (BLA) | August 13, 2010 |
| Xyntha | 58394-015 | Kit | Biologics (BLA) | August 1, 2008 |
| Xyntha | 58394-014 | Kit | Biologics (BLA) | August 1, 2008 |
| Xyntha | 58394-013 | Kit | Biologics (BLA) | August 1, 2008 |
| Xyntha | 58394-012 | Kit | Biologics (BLA) | August 1, 2008 |
| BeneFIX | 58394-636 | Kit | Biologics (BLA) | July 6, 2007 |
| Coagulation factor ix recombinant human | 58394-789 | Liquid | Bulk ingredients | February 1, 1997 |
| BeneFIX | 58394-635 | Kit | Biologics (BLA) | February 1, 1997 |
| BeneFIX | 58394-634 | Kit | Biologics (BLA) | February 1, 1997 |
| BeneFIX | 58394-633 | Kit | Biologics (BLA) | February 1, 1997 |
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.