FDA Drug recall D-0007-2015
ZyGenerics ATENOLOL Tablets, USP 25 mg 1000 count bottle, Rx Only Manufactured by: Cadila Healthcare Ltd
- FDA Drug
- Class II
- terminated
- Published 2014-10-15
On 2014-10-15 the FDA classified a Class II recall of ZyGenerics ATENOLOL Tablets, USP 25 mg 1000 count bottle, Rx Only Manufactured by: Cadila Healthcare Ltd by Zydus Pharmaceuticals Usa, citing superpotent Drug: A complaint was reported by a pharmacist who stated several tablets were noticeably thicker in appearance.
Read the official FDA Drug notice
| Agency | FDA Drug |
|---|---|
| Recall number | D-0007-2015 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2014-08-05 |
| Published | 2014-10-15 |
| Last updated | 2026-09-13 11:51 UTC |
| Company | Zydus Pharmaceuticals Usa |
| Distribution | US |
Product
ZyGenerics ATENOLOL Tablets, USP 25 mg 1000 count bottle, Rx Only Manufactured by: Cadila Healthcare Ltd. Ahmedabad, India Distributed by: Zydus Pharmaceuticals USA Inc. Pennington, NJ 08634 USA NDC 68382-022-01
Reason
Superpotent Drug: A complaint was reported by a pharmacist who stated several tablets were noticeably thicker in appearance.
Identifiers
| ndc | 68382-022-16 |
|---|---|
| ndc | 68382-022-01 |
| ndc | 68382-022-10 |
| ndc | 68382-022-40 |
| ndc | 68382-022-24 |
| ndc | 68382-023-16 |
| ndc | 68382-023-01 |
| ndc | 68382-023-10 |
| ndc | 68382-023-02 |
| ndc | 68382-023-40 |
| ndc | 68382-023-24 |
| ndc | 68382-024-16 |
| ndc | 68382-024-01 |
| ndc | 68382-024-10 |
| ndc | 68382-024-40 |
| code_info | MP2292 Exp. 01/16 |
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:51 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-0007-2015%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.