# FDA recall D-329-2013

> **Glenmark Generics Inc., USA** · Class III · drug recall initiated 2013-04-05.

## Product

Glenmark Gabapentin Tablets, a) 600mg, 500- count bottle   (NDC 68462-126-05), b) 800 mg, 500- count bottle (NDC 68462-127-05), Rx only, Manufactured by Glenmark Generics Ltd.Colvale- Bardez Ltd 403513, India, Manufactured for :  Glenmark Generics USA Mahwah, NJ 07430.

## Reason for recall

Chemical Contamination: Gabapentin Sodium tablets is recalled due to complaints related to an off - odor described as moldy, musty or fishy in nature.

## Distribution

Nationwide

## Key facts

- **Recall number:** D-329-2013
- **Recalling firm:** Glenmark Generics Inc., USA
- **Classification:** Class III
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2013-04-05
- **Report date:** 2013-05-22
- **Termination date:** 2014-10-09

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Mahwah, NJ, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D-329-2013

## Citation

> AI Analytics. FDA recall D-329-2013. Retrieved 2026-05-26 from https://api.ai-analytics.org/recall/D-329-2013. Source: US FDA. Licensed CC0.

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