NDC 0008-1222
PristiqExtended-Release 100 mg tablet, extended release
On the label: Wyeth Pharmaceuticals LLC, a subsidiary of Pfizer Inc..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Pfizer Asia Manufacturing Pte Ltd | Singapore, Singapore | Makes the active ingredient and tests it | Problems found, fixed voluntarilyOct 18, 2023 · 6 inspections |
| Pfizer Ireland Pharmaceuticals Unlimited Company | Newbridge, Ireland | Makes it, tests it, packages it and labels it | Problems found, fixed voluntarilySep 23, 2022 · 8 inspections |
| Pfizer Ireland Pharmaceuticals Unlimited Company | Ringaskiddy, Ireland | Makes the active ingredient and tests it | Problems found, fixed voluntarilyOct 25, 2024 · 6 inspections |
| Pfizer Manufacturing Deutschland GmbH | Freiburg im Breisgau, Germany | Tests it, packages it and labels it | Problems found, fixed voluntarilyJul 2, 2025 · 8 inspections |
| Pharmacia & Upjohn Company LLC | Kalamazoo, MI, United States | Labels it | Problems found, fixed voluntarilyJun 16, 2023 · 9 inspections |
| Wyeth Pharmaceutical Division of Wyeth Holdings LLC | Pearl River, NY, United States | Tests it | Problems found, fixed voluntarilyDec 17, 2025 · 3 inspections |
Recalls
- Apr 16, 2014 · Class II · Pfizer Us Pharmaceutical Group
Presence of Foreign Tablets/Capsules: Pfizer is recalling 50 mg Pristiq (desvenlafaxine) extended release tablets because a single Pristiq 100 mg tablet was found in a bottle of 50 mg Pristiq.
Lots: H74477, H74478, Exp. 03/16, H74479, H79766 Exp. 05/16
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Desvenlafaxine: every company that makes it
- Form
- tablet, extended release, oral
- Strength
- 100 mg
- Approval
- NDA NDA021992
- On the market since
- May 1, 2008
- Package NDCs
0008-1222-010008-1222-140008-1222-300008-1222-50- Official label
- DailyMed (National Library of Medicine), updated Apr 28, 2026
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