Disulfiram Tablets USP 250 mg, 100 tablet bottle, Rx only, Manufactured for TEVA Pharmaceuticals, USA, Sellersville, PA --- NDC 0093-5035-01
Reported: June 12, 2013 Initiated: March 19, 2013 #D-578-2013
Product Description
Disulfiram Tablets USP 250 mg, 100 tablet bottle, Rx only, Manufactured for TEVA Pharmaceuticals, USA, Sellersville, PA --- NDC 0093-5035-01
Reason for Recall
CGMP Deviation; cotton coil is missing in some packaged bottles
Details
- Recalling Firm
- Teva Pharmaceuticals USA, Inc.
- Units Affected
- 68,322 bottles
- Distribution
- Nationwide
- Location
- Sellersville, PA
Frequently Asked Questions
What product was recalled? ▼
Disulfiram Tablets USP 250 mg, 100 tablet bottle, Rx only, Manufactured for TEVA Pharmaceuticals, USA, Sellersville, PA --- NDC 0093-5035-01. Recalled by Teva Pharmaceuticals USA, Inc.. Units affected: 68,322 bottles.
Why was this product recalled? ▼
CGMP Deviation; cotton coil is missing in some packaged bottles
Which agency issued this recall? ▼
This recall was issued by the FDA Drug on June 12, 2013. Severity: Low. Recall number: D-578-2013.
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