Venlafaxine Hydrochloride, Extended Release Capsules, 150 mg, UD-100 Tablets per Box (10 x 10), Rx Only, Manufactured by: Teva Pharmaceuticals USA, 1090 Horsham Rd, North Wales, PA 19454, NDC 63739-0512-10
Reported: March 26, 2014 Initiated: March 3, 2014 #D-1167-2014
Product Description
Venlafaxine Hydrochloride, Extended Release Capsules, 150 mg, UD-100 Tablets per Box (10 x 10), Rx Only, Manufactured by: Teva Pharmaceuticals USA, 1090 Horsham Rd, North Wales, PA 19454, NDC 63739-0512-10
Reason for Recall
Failed Dissolution Specification: Out of Specification dissolution results at 12 month interval.
Details
- Recalling Firm
- McKesson Packaging Services
- Units Affected
- 1,557 Boxes
- Distribution
- Nationwide
- Location
- Concord, NC
Frequently Asked Questions
What product was recalled? ▼
Venlafaxine Hydrochloride, Extended Release Capsules, 150 mg, UD-100 Tablets per Box (10 x 10), Rx Only, Manufactured by: Teva Pharmaceuticals USA, 1090 Horsham Rd, North Wales, PA 19454, NDC 63739-0512-10. Recalled by McKesson Packaging Services. Units affected: 1,557 Boxes.
Why was this product recalled? ▼
Failed Dissolution Specification: Out of Specification dissolution results at 12 month interval.
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on March 26, 2014. Severity: Low. Recall number: D-1167-2014.
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