Drug recall D-1060-2014
Product
Diclofenac Sodium and Misoprostol Delayed-Release Tablets, 75mg/0.2mg, Rx only, Manufactured by Watson Laboratories, Inc., Corona, CA 92880, NDC 0591-0398-60 (60 count bottles)
Reason for recall
Failed Tablet/Capsule Specifications: Broken tablets
Lots and codes
Lot 668271A, Exp 11/14 and Lot 684119A Exp 01/2015
Recall details
- Recalling firm
- Actavis Inc, Parsippany, NJ
- Quantity
- 6,540 bottles
- Distribution
- Nationwide
- Type
- Voluntary: Firm initiated
- Recall initiated
- March 22, 2013
- Terminated
- February 26, 2015
Related products
- Diclofenac sodium and Misoprostol – drug information
- NDC 0591-0397 Diclofenac Sodium and Misoprostol · Diclofenac Sodium 50 mg/1; Misoprostol 200 ug/1 · Actavis Pharma, Inc.
- NDC 0591-0398 Diclofenac Sodium and Misoprostol · Diclofenac Sodium 75 mg/1; Misoprostol 200 ug/1 · Actavis Pharma, Inc.