Drug recall D-0166-2024
Product
AMOXICILLIN Tablets, USP, 875MG, 20 Tablets, Rx Only, Manufactured by Sandoz GmbH for Sandoz Inc., Princeton, NJ 08540. NDC: 0781-5060-20
Reason for recall
CGMP Deviations: Products were exposed to temperatures outside of the products labeled storage conditions.
Lots and codes
Batch LJ9004
Recall details
- Recalling firm
- CARDINAL HEALTHCARE, Dublin, OH
- Quantity
- 2 units
- Distribution
- Nationwide USA
- Type
- Voluntary: Firm initiated
- Recall initiated
- January 26, 2022
- Terminated
- September 29, 2024
Related products
- Amoxicillin – drug information
- NDC 0781-6156 Amoxicillin · Amoxicillin 200 mg/5mL · Sandoz Inc
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- NDC 0781-5060 Amoxicillin · Amoxicillin 500 mg/1 · Sandoz Inc
- NDC 0781-6041 Amoxicillin · Amoxicillin 250 mg/5mL · Sandoz Inc
- NDC 0781-6157 Amoxicillin · Amoxicillin 400 mg/5mL · Sandoz Inc
- NDC 0781-6039 Amoxicillin · Amoxicillin 125 mg/5mL · Sandoz Inc
- NDC 0781-2020 Amoxicillin · Amoxicillin 250 mg/1 · Sandoz Inc
- NDC 0781-2613 Amoxicillin · Amoxicillin 500 mg/1 · Sandoz Inc