Venlafaxine 75 mg Tablet recall: Labeling Error
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…
Why was Venlafaxine 75 mg Tablet 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.
What should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
Lot # 94983; Exp 10/17
- Product
- 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…
- Recalling firm
- Bryant Ranch Prepack Inc.
- Quantity
- 21 bottles (910 extended release tablets)
- Distribution
- Nationwide
- Recall date
- May 11, 2016
- Classification
- Class III
- Status
- Terminated
- Agency
- FDA (drug)