Class II
Terminated
Glipizide 2.5 mg Extended-release tablets, 30-count bottle, Rx Only, Manufactured By: Patheon Pharmaceuticals Inc Cincinnati, OH 45237, NDC 00591-0900-30
- Company
- Actavis Inc
- Recall Initiated
- June 30, 2016
- Posted
- August 24, 2016
- Recall Number
- D-1457-2016
- Voluntary / Mandated
- Voluntary: Firm initiated
- Quantity
- 167,152 bottles
- Firm Location
- Parsippany, NJ, United States
Reason for Recall
Failed Dissolution Specifications: Glipizide 2.5 mg ER Tablets exceeded dissolution specification rates for the 10 hour testing point.
Distribution
Nationwide
Lot / Code Info
Lot # 3132593, 3132594, 3134420, 3134421,3134422, Exp. 02/17
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