Drug recall D-1702-2012
Product
Levetiracetam Tablets, USP 500 mg, 500 count bottle, Rx only, Manufactured for: Mylan Pharmaceuticals Inc. Morgantown, WV 26505 USA, NDC 0378-5615-05
Reason for recall
Adulterated Presence of Foreign Tablets: Pharmaceutical manufacturer may have distributed foreign tablets in bottles of Levetiracetam Tablets, USP 500 mg.
Lots and codes
Lot ZLMM12063, Exp March 2014
Recall details
- Recalling firm
- Mylan Pharmaceuticals Inc., Morgantown, WV
- Quantity
- 960 bottles
- Distribution
- The product was distributed to KY.
- Type
- Voluntary: Firm initiated
- Recall initiated
- July 27, 2012
- Terminated
- May 21, 2013
Related products
- Levetiracetam – drug information
- NDC 0378-5619 Levetiracetam · Levetiracetam 1000 mg/1 · Mylan Pharmaceuticals Inc.
- NDC 0378-5617 Levetiracetam · Levetiracetam 750 mg/1 · Mylan Pharmaceuticals Inc.
- NDC 0378-5615 Levetiracetam · Levetiracetam 500 mg/1 · Mylan Pharmaceuticals Inc.