Gabapentin recall

Gabapentin Recalled Due to Empty Capsules A drug therapy for epilepsy and shingles pain is being voluntarily recalled by its manufacturer due

. Unclassified Recall; The recall has been initiated because the product lot has been found to contain some empty capsules. Gabapentin is

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 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 .

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 and it is currently ongoing.

Product recall Mock recall Remediation Retention Brand protection gabapentinoids (e.g. gabapentin and Lyrica, also known as pregabalin).

Aurobindo Recalls Gabapentin for Empty Capsules Aurobindo Pharma USA has issued a voluntary recall of its 300mg, 100-count bottles of

This recall is specific only to a has been impacted by the recall. Antispastics Gabapentin is available in brand-name and generic versions.