Drug recall D-1056-2017
Product
Famotidine Tablets USP, 20 mg, 100 count bottles, Rx only, Manufactured For: TEVA PHARMACEUTICALS USA, Sellersville, PA --- NDC 0172-5728-60
Reason for recall
Failed Tablet/Capsule Specification; out of specification for tablet weight
Lots and codes
Lot # 3429066, exp 06/2018
Recall details
- Recalling firm
- Teva Pharmaceuticals USA, North Wales, PA
- Quantity
- 28,188 bottles
- Distribution
- Nationwide
- Type
- Voluntary: Firm initiated
- Recall initiated
- July 24, 2017
- Terminated
- January 31, 2018
Related products
- Famotidine – drug information
- NDC 0172-5728 Famotidine · Famotidine 20 mg/1 · Teva Pharmaceuticals USA, Inc.
- NDC 0172-5729 Famotidine · Famotidine 40 mg/1 · Teva Pharmaceuticals USA, Inc.