Class II · Moderate risk
Desvenlafaxine Extended-Release Tablets 25 mg 30 Tablets Rx Only…
CGMP Deviations: Intermittent exposure to temperature excursion during storage.
National Drug Code
Is NDC 0591-4060-30 recalled?
Desvenlafaxine · 30 TABLET, EXTENDED RELEASE in 1 BOTTLE (0591-4060-30)
Yes — this exact package was recalled
1 FDA recall names the code 0591-4060-30 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
- Strength
- DESVENLAFAXINE SUCCINATE 25 mg/1
- Form
- Tablet, Extended Release · Oral
- Labeler
- Actavis Pharma, Inc.
- Type
- Human Prescription Drug
- Product code
- 0591-4060
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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