Glenmark Gabapentin Tablets — Class III drug recall D-329-2013
Terminated recall by Glenmark Generics Inc., USA, reported 2013-05-22, distributed nationwide. Chemical Contamination: Gabapentin Sodium tablets is recalled due to complaints related to an off - odor descr
| Recall number | D-329-2013 |
|---|---|
| Product type | Drug |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Glenmark Generics Inc., USA, Mahwah, NJ, United States |
| Recall initiated | 2013-04-05 |
| Classified | 2013-05-16 |
| Reported by FDA | 2013-05-22 |
| Terminated | 2014-10-09 |
| Distributed | Nationwide (US) |
| Reason classes | chemical contamination |
| NDC | 68462-0126, 68462-0126-01, 68462-0126-05, 68462-0127, 68462-0127-01, 68462-0127-05 |
| Lot numbers | 02123419, 02123424, 02123430, 02123440, 02123445, 02123454, 02123465, 02123492, 02123523, 02123527, 02123532, 02123542, 02123546, 02123551, 02123555, 02123560, 02123566, 02123569, 02123789, 02123804, 02123821, 02123829, 02123834, 02123841, 02123845, 10/14, 11/14 |
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.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/D-329-2013. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.