Register entry
Wyeth Pharmaceuticals LLC, a subsidiary of Pfizer Inc.
Data as of · How to read this entry
- Registered sites
- 10
- Active NDC listings
- 30
- Live patents
- 2
- Countries
- 5
- Base
- United States
Authorisation
Registered operations
Analytical testing10Active ingredient (API) manufacture7Labelling4Finished drug manufacture7Packaging7
Sites
Registered establishments
10| Establishment | Address | Registered for | FEI / DUNS |
|---|---|---|---|
| Pfizer Canada ULCRegistrant: Wyeth Pharmaceuticals LLC, a subsidiary of Pfizer Inc. | 720 17th St E, Brandon, Manitoba R7A 7H2, Canada (CAN) | Analytical testing, Active ingredient (API) manufacture | 3002806438203382973 |
| Wyeth Farma SARegistrant: Wyeth Pharmaceuticals LLC, a subsidiary of Pfizer Inc. | Autovia del Norte A-1, KM 23, Desvio Algete KM 1, San Sebastian de los Reyes, M 28700, Spain (ESP) | Analytical testing, Labelling, Finished drug manufacture, Packaging | 3003973260462005232 |
| Pfizer Ireland Pharmaceuticals Unlimited CompanyRegistrant: Wyeth Pharmaceuticals LLC, a subsidiary of Pfizer Inc. | Grange Castle Business Park, Nangor Road, Dublin, D22 V8F8, Ireland (IRL) | Analytical testing, Active ingredient (API) manufacture, Finished drug manufacture, Packaging | 3004145594985586408 |
| Pfizer Ireland Pharmaceuticals Unlimited CompanyRegistrant: Wyeth Pharmaceuticals LLC, a subsidiary of Pfizer Inc. | Little Connell, Newbridge, W12 HX57, Ireland (IRL) | Analytical testing, Active ingredient (API) manufacture, Labelling, Finished drug manufacture, Packaging | 3006785053986019327 |
| Wyeth Lederle SRLRegistrant: Wyeth Pharmaceuticals LLC, a subsidiary of Pfizer Inc. | Via Franco Gorgone, Catania, 95121, Italy (ITA) | Analytical testing, Labelling, Finished drug manufacture, Packaging | 3002806766542812040 |
| Wyeth BioPharma Division of Wyeth Pharmaceuticals LLCRegistrant: Wyeth Pharmaceuticals LLC, a subsidiary of Pfizer Inc. | 1 Burtt Rd, Andover, Massachusetts (MA) 01810, United States (USA) | Analytical testing, Active ingredient (API) manufacture | 1222181174350868 |
| GenTrac Inc.Registrant: Wyeth Pharmaceuticals LLC, a subsidiary of Pfizer Inc. | 2232 Pleasant View Rd, Middleton, Wisconsin (WI) 53562, United States (USA) | Analytical testing, Active ingredient (API) manufacture | 3002919848058521017 |
| Wyeth Pharmaceutical Division of Wyeth Holdings LLCRegistrant: Wyeth Pharmaceuticals LLC, a subsidiary of Pfizer Inc. | 401 N Middletown Rd, Pearl River, New York (NY) 10965, United States (USA) | Analytical testing, Active ingredient (API) manufacture, Finished drug manufacture, Packaging | 2410662054065909 |
| King Pharmaceuticals LLCRegistrant: Wyeth Pharmaceuticals LLC, a subsidiary of Pfizer Inc. | 1200 Parkdale Rd, Rochester, Michigan (MI) 48307, United States (USA) | Analytical testing, Labelling, Finished drug manufacture, Packaging | 1876582962691478 |
| Wyeth Pharmaceutical Division of Wyeth Holdings LLCRegistrant: Wyeth Pharmaceuticals LLC, a subsidiary of Pfizer Inc. | 4300 Oak Park Rd, Sanford, North Carolina (NC) 27330, United States (USA) | Analytical testing, Active ingredient (API) manufacture, Finished drug manufacture, Packaging | 1000110954883534067 |
Catalogue
Drug listings by form and route
3030 active NDC listings: 30 human prescription drug. By marketing category: NDA 27, BLA 3.
| Dosage form | NDCs |
|---|---|
| tablet, film coated | 6 |
| injection, powder, lyophilized, for solution | 5 |
| tablet, sugar coated | 4 |
| injection, powder, for solution | 3 |
| injection, solution | 3 |
| tablet, extended release | 3 |
| kit | 2 |
| tablet, delayed release | 2 |
| cream | 1 |
| granule, delayed release | 1 |
| Route | NDCs |
|---|---|
| oral | 16 |
| intravenous | 11 |
| intramuscular | 1 |
| vaginal | 1 |
| Labeller name on the listing | NDCs |
|---|---|
| wyeth pharmaceuticals llc, a subsidiary of pfizer inc. | 30 |
Exclusivity
Patents and exclusivities
2| Patent | Product | Covers | Expiry |
|---|---|---|---|
| 7544370*PED | PROTONIXpantoprazole sodium | use | Dec 2026 |
| 7683051 | DUAVEEbazedoxifene acetate; estrogens, conjugated | substance, product | Mar 2027 |
Catalogue
Marketed products
30| Brand | Generic name | Form / route | NDC |
|---|---|---|---|
| Besponsa | inotuzumab ozogamicin | injection, powder, lyophilized, for solution, intravenous | 0008-0100BLA |
| Duavee | conjugated estrogens/bazedoxifene | tablet, film coated, oral | 0008-1123NDA |
| Mylotarg | gemtuzumab ozogamicin | injection, powder, lyophilized, for solution, intravenous | 0008-4510BLA |
| North American Coral Snake Antivenin (Equine) | Coral Snake (Micrurus Fulvius) Immune Globulin Antivenin (Equine) | injection, powder, for solution, intravenous | 0008-0423BLA |
| Premarin | CONJUGATED ESTROGENS | injection, powder, lyophilized, for solution, intramuscular, intravenous | 0046-0749NDA |
| Premarin | estrogens, conjugated | tablet, film coated, oral | 0046-1100NDA |
| Premarin | estrogens, conjugated | tablet, film coated, oral | 0046-1101NDA |
| Premarin | estrogens, conjugated | tablet, film coated, oral | 0046-1102NDA |
| Premarin | estrogens, conjugated | tablet, film coated, oral | 0046-1103NDA |
| Premarin | estrogens, conjugated | tablet, film coated, oral | 0046-1104NDA |
| Premarin Vaginal | conjugated estrogens | cream, vaginal | 0046-0872NDA |
| Premphase | conjugated estrogens and medroxyprogesterone acetate | kit | 0046-2575NDA |
| Prempro | conjugated estrogens and medroxyprogesterone acetate | tablet, sugar coated, oral | 0046-1105NDA |
| Prempro | conjugated estrogens and medroxyprogesterone acetate | tablet, sugar coated, oral | 0046-1106NDA |
| Prempro | conjugated estrogens and medroxyprogesterone acetate | tablet, sugar coated, oral | 0046-1107NDA |
| Prempro | conjugated estrogens and medroxyprogesterone acetate | tablet, sugar coated, oral | 0046-1108NDA |
| Pristiq Extended-Release | desvenlafaxine succinate | tablet, extended release, oral | 0008-1210NDA |
| Pristiq Extended-Release | desvenlafaxine succinate | tablet, extended release, oral | 0008-1211NDA |
| Pristiq Extended-Release | desvenlafaxine succinate | tablet, extended release, oral | 0008-1222NDA |
| Protonix Delayed-Release | PANTOPRAZOLE SODIUM | tablet, delayed release, oral | 0008-0841NDA |
| Protonix Delayed-Release | PANTOPRAZOLE SODIUM | tablet, delayed release, oral | 0008-0843NDA |
| Protonix Delayed-Release | PANTOPRAZOLE SODIUM | granule, delayed release, oral | 0008-0844NDA |
| Protonix I.V. | PANTOPRAZOLE SODIUM | injection, powder, for solution, intravenous | 0008-0923NDA |
| Protonix I.V. | PANTOPRAZOLE SODIUM | injection, powder, for solution, intravenous | 0008-4001NDA |
| Torisel | temsirolimus | kit | 0008-1179NDA |
| Tygacil | TIGECYCLINE | injection, powder, lyophilized, for solution, intravenous | 0008-4990NDA |
| Tygacil | TIGECYCLINE | injection, powder, lyophilized, for solution, intravenous | 0008-4994NDA |
| Zosyn in Galaxy Containers | TAZOBACTAM SODIUM and PIPERACILLIN SODIUM | injection, solution, intravenous | 0206-8860NDA |
| Zosyn in Galaxy Containers | TAZOBACTAM SODIUM and PIPERACILLIN SODIUM | injection, solution, intravenous | 0206-8861NDA |
| Zosyn in Galaxy Containers | TAZOBACTAM SODIUM and PIPERACILLIN SODIUM | injection, solution, intravenous | 0206-8862NDA |
Neighbours
Registered in the same town
12- Astellas Pharma US, Inc.DUBLIN, IRL; Sanford, NC · 2 sites
- Zoetis IncCATANIA, ITA
- Allergan, Inc.Dublin, IRL
- Takeda Pharmaceuticals U.S.A., Inc.Dublin, IRL
- Par Health USA, LLCRochester, MI
- West Pharmaceutical Services, Inc.Dublin, IRL
- Alexion Pharmaceuticals, Inc.Dublin, IRL
- COTY LANCASTER SAMSANFORD, NC
- Cambridge Isotope Laboratories, Inc.Andover, MA
- LEO Pharma A/SDublin, IRL
- PPD Development, L.P.Middleton, WI
- Scientific Protein Laboratories LLCPearl River, NY
Compare
Comparable companies in United States
- Eli Lilly and Company10 sites · 189 NDC
- Medical-technical Gases, Inc.10 sites · 7 NDC
- Alcami Carolinas Corporation10 sites · 1 NDC
- The Procter & Gamble Manufacturing Company11 sites · 849 NDC
- Amgen, Inc9 sites · 105 NDC
- Zoetis Inc11 sites · 29 NDC
- Pfizer Inc11 sites · 27 NDC
- Sotera Health LLC11 sites · 2 NDC
- Haleon US Holdings LLC8 sites · 405 NDC
- Genentech, Inc.8 sites · 93 NDC
Enquiry
Common questions
- Is Wyeth Pharmaceuticals LLC, a subsidiary of Pfizer Inc. FDA approved?
- Wyeth Pharmaceuticals LLC, a subsidiary of Pfizer Inc. holds 10 FDA-registered establishments across 5 countries. Registration puts a site on the FDA's register and open to inspection; it is not an approval of the company. Approvals attach to individual drug applications.
- Where are Wyeth Pharmaceuticals LLC, a subsidiary of Pfizer Inc.'s drugs manufactured?
- At registered sites in Canada, Spain, Ireland, Italy, the United States. The FDA register lists Brandon; San Sebastian de los Reyes; Dublin; Newbridge; Catania; Andover, MA, and 4 more. Registered operations: analytical testing, active ingredient (API) manufacture, labelling, finished drug manufacture, packaging.
- What drugs does Wyeth Pharmaceuticals LLC, a subsidiary of Pfizer Inc. make?
- 30 products are listed under Wyeth Pharmaceuticals LLC, a subsidiary of Pfizer Inc. in the openFDA NDC Directory, most often as tablet, film coated; injection, powder, lyophilized, for solution; tablet, sugar coated. The full breakdown by dosage form and route is above. A listing count is not a sales figure.
Compiled from FDA establishment registrations, the openFDA NDC Directory, the Orange Book and the FDA drug shortage database. Not claimed by the company. Sources and methodology.