drugs Class III Updated 2013-01-23

Teva Pharmaceuticals USA, Inc. recalls CABERGOLINE Tablets, 0.5 mg, RX only, 8 count bottles, Manuf

Recalled Product

CABERGOLINE Tablets, 0.5 mg, RX only, 8 count bottles, Manufactured For: TEVA PHARMACEUTICALS USA, Sellersville, PA 18960 NDC 0093-5420-88

Hazard / Issue

Impurities/Degradation Products: This lot of product will not meet the impurity specification over shelf life

Issued by

FDA

Distribution: Nationwide (United States)
Lot/Code Info: Lot number 6A007046V, exp 07/12
View official government recall

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