Class III ยท Low risk
Venlafaxine 75 mg Tablet
Labeling: Label Mix-Up: Bryant Ranch received Tevas venlafaxine hydrochloride extended-release tablets for repackaging, but labeled it incorrectly as the immediate release formulation.
National Drug Code
Is NDC 63629-3324-06 recalled?
Venlafaxine · 100 TABLET in 1 BOTTLE (63629-3324-6)
Yes — this exact package was recalled
1 FDA recall names the code 63629-3324-06 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
- Venlafaxine
- Strength
- VENLAFAXINE HYDROCHLORIDE 75 mg/1
- Form
- Tablet · Oral
- Labeler
- Bryant Ranch Prepack
- Type
- Human Prescription Drug
- Product code
- 63629-3324
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
- 63629-1064 Spironolactone 1
- 63629-1067 Spironolactone 1
- 63629-1088 Morphine sulfate 1
- 63629-1089 Morphine sulfate 1
- 63629-6905 See recall 1
- 63629-6922 See recall 1
Free recall alerts
Know the day your medication is recalled
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