# FDA recall D-331-2013

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

## Product

Glenmark Topiramate Tablets, 200 mg,  60-count bottle, (NDC 68462-110-60), 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: Topiramate Tablets is being recalled due to complaints related to an off - odor. described as moldy, musty or fishy in nature.

## Distribution

Nationwide

## Key facts

- **Recall number:** D-331-2013
- **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-331-2013

## Citation

> AI Analytics. FDA recall D-331-2013. Retrieved 2026-05-26 from https://api.ai-analytics.org/recall/D-331-2013. Source: US FDA. Licensed CC0.

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