ALLOPURINOL Recall D-0583-2024
Description: Allopurinol Tablets, USP 300mg, 100 Tablets per bottle, Rx only, Manufactured By: Dr. Reddy's Laboratories LA LLC, Shreveport, LA 71106 USA, NDC 55111-730-01.
ALLOPURINOL Recall D-0583-2024 Information
| Status | Ongoing |
| Mandated? | Voluntary: Firm initiated |
| Recall Number | D-0583-2024 |
| Event ID | 94781 |
| Brand | ALLOPURINOL |
| Generic Name | ALLOPURINOL |
| Manufacturer | ALLOPURINOL |
| Original Package? | 1 |
| Active Substance | ALLOPURINOL |
| Drug Route | ORAL |
| Distribution | IL, MS, OH |
| Quantity | 20,520 units |
| Recall Reason | Presence of foreign substance. |
| Drug Classification | Class II |
| Drug Code Info | 20240710 |
| Product NDC | 55111-729 55111-730 |
| Product NUI | N0000175698 N0000000206 |
| Pharma Class (EPC) | Xanthine Oxidase Inhibitor [EPC] |
| Recall Initiation Date | 20240607 |
| Report Date | 20240710 |
| Classification Date | 20240703 |
| Address | 107 College Rd EN/A Princeton, NJ 08540-6623 United States |
| Recalling Firm | Dr. Reddy's Laboratories, Inc. |
| Initial Notification | Letter |
| Unique Ingredient Identifier | 63CZ7GJN5I |
| Drug Application Number | ANDA071586 |
| Structured Product Labeling (SPL ID) | 0837a638-aa97-b433-6fa4-cd4adf3bc82c |
| Structured Product Labeling (SPL Set ID) | 19a138b8-d225-03e6-f762-abe71560204b |
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