Class II · Moderate risk
Pristiq (desvenlafaxine)
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.
National Drug Code
Is NDC 0008-1211-30 recalled?
Pristiq Extended-Release · 30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (0008-1211-30)
Yes — this exact package was recalled
1 FDA recall names the code 0008-1211-30 directly. A recall still applies to particular lot numbers — compare the lot on your package with the FDA notice below, and talk to your pharmacist before stopping a prescribed medication.
- Active ingredient
- desvenlafaxine succinate
- Strength
- DESVENLAFAXINE SUCCINATE 50 mg/1
- Form
- Tablet, Extended Release · Oral
- Labeler
- Wyeth Pharmaceuticals LLC, a subsidiary of Pfizer Inc.
- Type
- Human Prescription Drug
- Product code
- 0008-1211
Recalls naming this package
Where to find this code. The NDC is printed on the pharmacy label and on the manufacturer's carton, usually as three groups of digits after “NDC”. The last group is the package size — two bottles of the same medicine can differ only in that group, and a recall may cover one but not the other.
Other recalled products from this labeler
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