FDAFDA · Food and drugs·Recall number D-1167-2014
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
Published March 26, 2014 · Recall initiated: March 3, 2014
Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.
What's the hazard
Failed Dissolution Specification: Out of Specification dissolution results at 12 month interval.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- McKesson Packaging Services
- Distributor
- Nationwide
- Lot
- Lot #: 91357
- Risk classification
- Class III
- Area (FDA)
- drug
- Country
- United States
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