AMPICILLIN SODIUM Recall D-0591-2023
Description: Ampicillin and Sulbactam for Injection, USP 3 gram per vial, Rx only, Manufactured for: Civica Inc. Lehi Utah 84043, NDC 72572-022-10
AMPICILLIN SODIUM Recall D-0591-2023 Information
| Status | Ongoing |
| Mandated? | Voluntary: Firm initiated |
| Recall Number | D-0591-2023 |
| Event ID | 92341 |
| Brand | AMPICILLIN AND SULBACTAM |
| Generic Name | AMPICILLIN AND SULBACTAM |
| Manufacturer | AMPICILLIN AND SULBACTAM |
| Original Package? | 1 |
| Active Substance | AMPICILLIN SODIUM SULBACTAM SODIUM |
| Drug Route | INTRAMUSCULAR |
| Distribution | Nationwide within the United States |
| Quantity | 419,680 vials |
| Recall Reason | Lack of Assurance of Sterility |
| Drug Classification | Class II |
| Drug Code Info | 20230524 |
| Product NDC | 72572-021 72572-022 |
| Recall Initiation Date | 20230515 |
| Report Date | 20230524 |
| Classification Date | 20230518 |
| Address | 911 G I D C Makarpura Vadodara, India |
| Recalling Firm | Astral SteriTech Private Ltd. |
| Initial Notification | Letter |
| Unique Ingredient Identifier | JFN36L5S8K DKQ4T82YE6 |
| Drug Application Number | ANDA090579 |
| Structured Product Labeling (SPL ID) | 29b2046c-a9eb-4dac-8322-20ff4a6c1f73 |
| Structured Product Labeling (SPL Set ID) | 1826e630-5305-4d76-91d6-009ed1caef4d |
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