Data / Drug companies / Wyeth Pharmaceuticals LLC, a Subsidiary of Pfizer Inc.
Wyeth Pharmaceuticals LLC, a Subsidiary of Pfizer Inc.: 15 products in the FDA NDC directory, labeler code 0008
Updated November 6, 2026. Source: US Food and Drug Administration, National Drug Code Directory (openFDA).
Wyeth Pharmaceuticals LLC, a Subsidiary of Pfizer Inc. (labeler code 0008) lists 15 products in the FDA National Drug Code Directory, covering 7 finished drugs by generic name. By type: 15 prescription drugs. Its main marketing category is new drug applications (NDA). The newest product started marketing on September 7, 2017.
The request: Watch Wyeth Pharmaceuticals LLC, a Subsidiary of Pfizer Inc. (FDA labeler code 0008): each new product listing and each discontinued product. $10 of work on sign-up, no card.
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- Labeler code
- 0008
- Products in commercial distribution
- 15
- Packages
- 24
- Finished drugs by generic name
- 7
- Prescription products
- 15
- Over the counter products
- 0
- Flagged as original packager
- 15 of 15 products that carry the flag
- Started marketing in the last 12 months
- 0
- Earliest marketing start
- May 1, 2000
- openFDA record search
- api.fda.gov
Products by marketing category
Share of the company's products in commercial distribution.
| Marketing category | Products | Share |
|---|---|---|
| New drug applications (NDA) | 12 | 80% |
| Biologics (BLA) | 3 | 20% |
Products by type
| Type | Products | Share |
|---|---|---|
| Prescription drugs | 15 | 100% |
Drugs it lists
Finished drugs by generic name, with how many companies list each.
| Drug | Products | Companies listing it |
|---|---|---|
| Pantoprazole sodium | 5 | 54 |
| Desvenlafaxine succinate | 3 | 12 |
| Tigecycline | 2 | 6 |
| Inotuzumab ozogamicin | 1 | 1 |
| Temsirolimus | 1 | 3 |
| Gemtuzumab ozogamicin | 1 | 1 |
| Conjugated estrogens/bazedoxifene | 1 | 2 |
Dosage forms
| Dosage form | Products | Share |
|---|---|---|
| Injection, powder, lyophilized, for solution | 4 | 26.7% |
| Tablet, extended release | 3 | 20% |
| Injection, powder, for solution | 3 | 20% |
| Tablet, delayed release | 2 | 13.3% |
| Kit | 1 | 6.7% |
| Granule, delayed release | 1 | 6.7% |
| Tablet, film coated | 1 | 6.7% |
Pharmacologic classes
FDA established pharmacologic classes of its products.
| Class | Products |
|---|---|
| Proton Pump Inhibitor | 5 |
| Serotonin and Norepinephrine Reuptake Inhibitor | 3 |
| Tetracycline-class Antibacterial | 2 |
| CD22-directed Immunoconjugate | 1 |
| CD33-directed Immunoconjugate | 1 |
| Estrogen | 1 |
| Estrogen Agonist/Antagonist | 1 |
Newest products
By marketing start date.
| Product | Product NDC | Dosage form | Marketing category | Marketing start |
|---|---|---|---|---|
| Mylotarg | 0008-4510 | Injection, powder, lyophilized, for solution | Biologics (BLA) | September 7, 2017 |
| Besponsa | 0008-0100 | Injection, powder, lyophilized, for solution | Biologics (BLA) | August 18, 2017 |
| Tygacil | 0008-4994 | Injection, powder, lyophilized, for solution | New drug applications (NDA) | February 8, 2017 |
| North American Coral Snake Antivenin (Equine) | 0008-0423 | Injection, powder, for solution | Biologics (BLA) | October 12, 2016 |
| Pristiq Extended-Release | 0008-1210 | Tablet, extended release | New drug applications (NDA) | April 1, 2015 |
| Duavee | 0008-1123 | Tablet, film coated | New drug applications (NDA) | October 3, 2013 |
| Protonix I.V. | 0008-4001 | Injection, powder, for solution | New drug applications (NDA) | May 1, 2013 |
| Tygacil | 0008-4990 | Injection, powder, lyophilized, for solution | New drug applications (NDA) | June 15, 2008 |
| Pristiq Extended-Release | 0008-1222 | Tablet, extended release | New drug applications (NDA) | May 1, 2008 |
| Pristiq Extended-Release | 0008-1211 | Tablet, extended release | New drug applications (NDA) | May 1, 2008 |
| Protonix Delayed-Release | 0008-0844 | Granule, delayed release | New drug applications (NDA) | February 29, 2008 |
| Torisel | 0008-1179 | Kit | New drug applications (NDA) | July 1, 2007 |
| Protonix I.V. | 0008-0923 | Injection, powder, for solution | New drug applications (NDA) | May 1, 2001 |
| Protonix Delayed-Release | 0008-0843 | Tablet, delayed release | New drug applications (NDA) | May 1, 2000 |
| Protonix Delayed-Release | 0008-0841 | Tablet, delayed release | New drug applications (NDA) | May 1, 2000 |
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.