The Drug Recall Report is for prescription drugs that are have recently been issued recalls by the U.S. Food and Drug Administration (FDA). Gabapentin 100mg
The last Recall Enforcement Report for Gabapentin with NDC was initiated on as a Class III recall due to product mixup: one foreign
The last Recall Enforcement Report for Gabapentin with NDC was initiated on as a Class II recall due to presence of foreign tablets; 3 fused tablets of metformin er 500 mg were found in bottle of gabapentin tablets The latest recall number for this product is D- and the recall is currently ongoing .
Aurobindo Recalls Gabapentin for Empty Capsules Aurobindo Pharma USA has issued a voluntary recall of its 300mg, 100-count bottles of
recall was deemed necessary. Another reason for the recall could be related to the formulation or manufacturing process of gabapentin. If there
FDA Recall Enforcement Reports. The last Recall Enforcement Report for Gabapentin with NDC was initiated on as a Class II recall due to presence of foreign tablets; 3 fused tablets of metformin er 500 mg were found in bottle of gabapentin tablets The latest recall number for this product is D- and the recall is
by CMM TRIMBLE 2024 Cited by 58Following baseline assessment, 15 patients were started on gabapentin as add-on therapy. (gabapentin order: VM (Immediate Recall, Best Recall, Recogni- tion)
Recalled: Northstar Label Gabapentin Capsules USP 300mg. FDA Recall Notice. sold at: Target Stores. recall date: . Recall Description. For more
The last Recall Enforcement Report for Gabapentin with NDC was initiated on as a Class II recall and it is currently ongoing.
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