Ranitidine Tablets USP — Class II drug recall D-1229-2014
Terminated recall by Glenmark Generics Inc., USA, reported 2014-04-16, distributed nationwide. Presence of Foreign Tablets/Capsules: Recall is due to a pharmacist complaint of a "foreign material", identif
| Recall number | D-1229-2014 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Glenmark Generics Inc., USA, Mahwah, NJ, United States |
| Recall initiated | 2014-03-18 |
| Classified | 2014-04-09 |
| Reported by FDA | 2014-04-16 |
| Terminated | 2015-01-21 |
| Distributed | Nationwide (US) |
| Quantity | 2,904 bottles |
| Reason classes | foreign material |
| UPC / GTIN / UDI-DI | 00368462248058 |
| NDC | 68462-0248-05 |
| Lot numbers | 10/14, 12AN118A |
Product
Ranitidine Tablets USP, 150 mg, 500-count bottles, Rx only, Manufactured by: Shasun Pharmaceuticals Limited, Unit-II R.S. No 32 33 & 34, Shasun Road, Periyakalapet, Puducherry, - 605 014, India; Manufactured for: Glenmark Generics Inc, USA, Mahwah, NJ 07430, UPC 3 68462 24805 8, NDC 68462-248-05.
Reason for recall
Presence of Foreign Tablets/Capsules: Recall is due to a pharmacist complaint of a "foreign material", identified as Metoprolol Tartrate Tablet USP 50 mg, found co-mingled in a bottle of Ranitidine Tablets USP 150 mg.
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-1229-2014. 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.