Drug recall D-128-2013
Product
CABERGOLINE Tablets, 0.5 mg, RX only, 8 count bottles, Manufactured For: TEVA PHARMACEUTICALS USA, Sellersville, PA 18960 NDC 0093-5420-88
Reason for recall
Impurities/Degradation Products: This lot of product will not meet the impurity specification over shelf life
Lots and codes
Lot number 6A007046V, exp 07/12
Recall details
- Recalling firm
- Teva Pharmaceuticals USA, Inc., Sellersville, PA
- Quantity
- 13,232 bottles
- Distribution
- Nationwide
- Type
- Voluntary: Firm initiated
- Recall initiated
- April 24, 2012
- Terminated
- December 18, 2013
Related products
- Cabergoline – drug information
- NDC 0093-5420 Cabergoline · Cabergoline .5 mg/1 · Teva Pharmaceuticals USA, Inc.