US Drug Recall Register
Class III · Low risk Terminated Initiated Mar 3, 2014 (13 years ago)

Venlafaxine Hydrochloride, Extended Release Capsules, 150 mg, UD-100 Tablets per Box (10…

Class III — Low risk. Unlikely to cause harm, but violates FDA regulations.

Why it was recalled

Failed Dissolution Specification: Out of Specification dissolution results at 12 month interval.

What 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

Recalling firm
McKesson Packaging Services
NDC code
63739-0512-10
Origin
NC, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-1167-2014

What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.

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