Class II · Moderate risk
Venlafaxine Hydrochloride Extended-Release Capsules
Failed Dissolution Specifications: Out-of-specification results observed for dissolution testing at the 8-hour and 12-hour pull intervals.
National Drug Code
Is NDC 68382-0034-10 recalled?
venlafaxine hydrochloride · 1000 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (68382-034-10)
Yes — this exact package was recalled
1 FDA recall names the code 68382-0034-10 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 hydrochloride
- Strength
- VENLAFAXINE HYDROCHLORIDE 37.5 mg/1
- Form
- Capsule, Extended Release · Oral
- Labeler
- Zydus Pharmaceuticals USA Inc.
- Type
- Human Prescription Drug
- Product code
- 68382-0034
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
- 68382-0021 Venlafaxine 2
- 68382-0033 See recall 2
- 68382-0095 Carvedilol 2
- 68382-0099 Paroxetine 2
- 68382-0110 Bromocriptine mesylate 2
- 68382-0123 Amlodipine Besylate 2
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