Isoniazid Tablets 300 mg tablets USP — Class II drug recall D-174-2013
Terminated recall by West-ward Pharmaceutical Corp., reported 2013-03-06, distributed in GA. Failed Dissolution Specifications; 36 month stability timepoint
| Recall number | D-174-2013 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | West-ward Pharmaceutical Corp., Eatontown, NJ, United States |
| Recall initiated | 2012-12-04 |
| Classified | 2013-02-27 |
| Reported by FDA | 2013-03-06 |
| Terminated | 2014-01-14 |
| Distributed | GA |
| Quantity | 77,531 bottles |
| Reason classes | specification failure |
| NDC | 61748-0013-01, 61748-0013-30 |
Product
Isoniazid Tablets 300 mg tablets USP, Rx Only, a) 30 tablets - NDC 61748-013-30, b) 100 tablets - NDC 61748-013-01, Mfd for: VersaPharm Incorporated Marietta, GA 30065-1505, Mfd by: West - Ward Pharmaceutical Corp.., Eatontown, NJ 07724
Reason for recall
Failed Dissolution Specifications; 36 month stability timepoint
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-174-2013. 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.