FDAFDA · Food and drugs·Recall number D-202-2013
Venlafaxine Hydrochloride Tablets, 75 mg*, 100-count tablets per bottle, Rx only, Manufactured by: Cadila Healthcare Ltd., Ahmedabad, India; Distributed by: Zydus Pharmaceuticals USA Inc., Pennington, NJ 08534, NDC 68382-021-01.
Published April 3, 2013 · Recall initiated: March 5, 2013
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 Tablet/Capsule Specifications: Pharmacist complaint of an excessive amount of broken and/or chipped tablets in the bottle.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Brand
- VENLAFAXINE
- Manufacturer
- Zydus Pharmaceuticals USA Inc
- Distributor
- Nationwide.
- UPC
- 0368382019011
- Lot
- Lot #: MM8490, Exp 09/14
- Risk classification
- Class II
- Area (FDA)
- drug
- Country
- United States
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