FDA Drug recall D-202-2013
Venlafaxine Hydrochloride Tablets, 75 mg*, 100-count tablets per bottle, Rx only, Manufactured by: Cadila Healthcare Ltd., Ahmedabad, India
- FDA Drug
- Class II
- terminated
- Published 2013-04-03
On 2013-04-03 the FDA classified a Class II recall of Venlafaxine Hydrochloride Tablets, 75 mg*, 100-count tablets per bottle, Rx only, Manufactured by: Cadila Healthcare Ltd., Ahmedabad, India by Zydus Pharmaceuticals Usa, citing failed Tablet/Capsule Specifications: Pharmacist complaint of an excessive amount of broken and/or chipped tablets in the bottle.
Read the official FDA Drug notice
| Agency | FDA Drug |
|---|---|
| Recall number | D-202-2013 |
| Classification | Class II |
| Status | terminated |
| Initiated | 2013-03-05 |
| Published | 2013-04-03 |
| Last updated | 2026-09-13 11:51 UTC |
| Company | Zydus Pharmaceuticals Usa |
| Distribution | US |
Product
Venlafaxine Hydrochloride Tablets, 75 mg*, 100-count tablets per bottle, Rx only, Manufactured by: Cadila Healthcare Ltd., Ahmedabad, India; Distributed by: Zydus Pharmaceuticals USA Inc., Pennington, NJ 08534, NDC 68382-021-01.
Reason
Failed Tablet/Capsule Specifications: Pharmacist complaint of an excessive amount of broken and/or chipped tablets in the bottle.
Identifiers
| ndc | 68382-018-06 |
|---|---|
| ndc | 68382-018-14 |
| ndc | 68382-018-16 |
| ndc | 68382-018-01 |
| ndc | 68382-018-05 |
| ndc | 68382-018-10 |
| ndc | 68382-019-06 |
| ndc | 68382-019-14 |
| ndc | 68382-019-16 |
| ndc | 68382-019-01 |
| ndc | 68382-019-05 |
| ndc | 68382-019-10 |
| ndc | 68382-020-06 |
| ndc | 68382-020-14 |
| ndc | 68382-020-16 |
| ndc | 68382-020-01 |
| ndc | 68382-020-05 |
| ndc | 68382-020-10 |
| ndc | 68382-021-06 |
| ndc | 68382-021-14 |
| ndc | 68382-021-16 |
| ndc | 68382-021-01 |
| ndc | 68382-021-05 |
| ndc | 68382-021-10 |
| ndc | 68382-101-06 |
| ndc | 68382-101-14 |
| ndc | 68382-101-16 |
| ndc | 68382-101-01 |
| ndc | 68382-101-05 |
| ndc | 68382-101-10 |
| code_info | Lot #: MM8490, Exp 09/14 |
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-202-2013%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.