Venlafaxine 75 mg Tablet, Compare to Effexor 75 mg Tablet, a) 30-count bottle (NDC 636290-3324-2), b) 100-count bottle (NDC 63629-3324-6), Rx Only, Manufactured by Teva Pharmaceuticals USA, Inc. Packaged by Bryant Ranch.
Reported: May 11, 2016 Initiated: March 25, 2016 #D-0837-2016
Product Description
Venlafaxine 75 mg Tablet, Compare to Effexor 75 mg Tablet, a) 30-count bottle (NDC 636290-3324-2), b) 100-count bottle (NDC 63629-3324-6), Rx Only, Manufactured by Teva Pharmaceuticals USA, Inc. Packaged by Bryant Ranch.
Reason for Recall
Labeling: Label Mix-Up: Bryant Ranch received Tevas venlafaxine hydrochloride extended-release tablets for repackaging, but labeled it incorrectly as the immediate release formulation.
Details
- Recalling Firm
- Bryant Ranch Prepack Inc.
- Units Affected
- 21 bottles (910 extended release tablets)
- Distribution
- Nationwide
- Location
- Burbank, CA
Frequently Asked Questions
What product was recalled? ▼
Venlafaxine 75 mg Tablet, Compare to Effexor 75 mg Tablet, a) 30-count bottle (NDC 636290-3324-2), b) 100-count bottle (NDC 63629-3324-6), Rx Only, Manufactured by Teva Pharmaceuticals USA, Inc. Packaged by Bryant Ranch.. Recalled by Bryant Ranch Prepack Inc.. Units affected: 21 bottles (910 extended release tablets).
Why was this product recalled? ▼
Labeling: Label Mix-Up: Bryant Ranch received Tevas venlafaxine hydrochloride extended-release tablets for repackaging, but labeled it incorrectly as the immediate release formulation.
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on May 11, 2016. Severity: Low. Recall number: D-0837-2016.
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