Diltiazem Hydrochloride Extended-Release Capsules — Class II drug recall D-0472-2024
Ongoing recall by Glenmark Pharmaceuticals Inc., USA, reported 2024-05-01, distributed nationwide. Failed Dissolution Specifications
| Recall number | D-0472-2024 |
|---|---|
| Product type | Drug |
| Classification | Class II |
| Status | Ongoing |
| Voluntary or mandated | Voluntary |
| Recalling firm | Glenmark Pharmaceuticals Inc., USA, Mahwah, NJ, United States |
| Recall initiated | 2024-04-17 |
| Classified | 2024-04-25 |
| Reported by FDA | 2024-05-01 |
| Distributed | Nationwide (US) |
| Quantity | 3,264 bottles |
| Reason classes | specification failure |
| NDC | 68462-0562, 68462-0562-01, 68462-0850, 68462-0850-01, 68462-0851, 68462-0851-01 |
| Lot numbers | 17221312 |
| Expiration dates | 2024-05-31 |
Product
Diltiazem Hydrochloride Extended-Release Capsules, USP 120 mg, Twice-a-Day Dosage, 100 Capsules per bottle, Rx Only, Manufactured for: Glenmark Pharmaceuticals Inc., USA Mahwah, NJ, 07430, Product of India, NDC 68462-562-01.
Reason for recall
Failed Dissolution Specifications
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-0472-2024. 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.