Drug recall D-202-2013
Product
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.
Reason for recall
Failed Tablet/Capsule Specifications: Pharmacist complaint of an excessive amount of broken and/or chipped tablets in the bottle.
Lots and codes
Lot #: MM8490, Exp 09/14
Recall details
- Recalling firm
- Zydus Pharmaceuticals USA Inc, Pennington, NJ
- Quantity
- 13,320 bottles
- Distribution
- Nationwide.
- Type
- Voluntary: Firm initiated
- Recall initiated
- March 5, 2013
- Terminated
- May 4, 2015
Related products
- Venlafaxine – drug information
- NDC 68382-021 Venlafaxine · Venlafaxine Hydrochloride 75 mg/1 · Zydus Pharmaceuticals USA Inc.
- NDC 68382-020 Venlafaxine · Venlafaxine Hydrochloride 50 mg/1 · Zydus Pharmaceuticals USA Inc.
- NDC 68382-019 Venlafaxine · Venlafaxine Hydrochloride 37.5 mg/1 · Zydus Pharmaceuticals USA Inc.
- NDC 68382-018 Venlafaxine · Venlafaxine Hydrochloride 25 mg/1 · Zydus Pharmaceuticals USA Inc.
- NDC 68382-101 Venlafaxine · Venlafaxine Hydrochloride 100 mg/1 · Zydus Pharmaceuticals USA Inc.