CABERGOLINE Tablets, 0.5 mg, RX only, 8 count bottles, Manufactured For: TEVA PHARMACEUTICALS USA, Sellersville, PA 18960 NDC 0093-5420-88
Reported: January 23, 2013 Initiated: April 24, 2012 #D-128-2013
Product Description
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
Details
- Recalling Firm
- Teva Pharmaceuticals USA, Inc.
- Units Affected
- 13,232 bottles
- Distribution
- Nationwide
- Location
- Sellersville, PA
Frequently Asked Questions
What product was recalled? ▼
CABERGOLINE Tablets, 0.5 mg, RX only, 8 count bottles, Manufactured For: TEVA PHARMACEUTICALS USA, Sellersville, PA 18960 NDC 0093-5420-88. Recalled by Teva Pharmaceuticals USA, Inc.. Units affected: 13,232 bottles.
Why was this product recalled? ▼
Impurities/Degradation Products: This lot of product will not meet the impurity specification over shelf life
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on January 23, 2013. Severity: Low. Recall number: D-128-2013.
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