Class III
Terminated
Disulfiram Tablets USP 250 mg, 100 tablet bottle, Rx only, Manufactured for TEVA Pharmaceuticals, USA, Sellersville, PA --- NDC 0093-5035-01
- Company
- Teva Pharmaceuticals Usa, Inc.
- Recall Initiated
- March 19, 2013
- Posted
- June 12, 2013
- Recall Number
- D-578-2013
- Voluntary / Mandated
- Voluntary: Firm initiated
- Quantity
- 68,322 bottles
- Firm Location
- Sellersville, PA, United States
Reason for Recall
CGMP Deviation; cotton coil is missing in some packaged bottles
Distribution
Nationwide
Lot / Code Info
NDC 0093-5035-01, Lot numbers 14064211A, exp 3/2014; 14064311A, exp 3/2014; 14064411A, exp 3/2014; 14064511A, exp 3/2014; 14090312A, exp 4/2015; 14092512A, exp 4/2015; 14092712A, exp 4/2015; 14094612A, exp 4/2015; 14099412A, exp 4/2015; 14099612B, exp 4/2015; 14099712A, exp 5/2015; 14110111A, exp 5/2014; 14110211A, exp 5/2014; 14110311A, exp 5/2014; 14110411A, exp 5/2014 and 34090212A, exp 4/2015.
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