FDA Drug recall D-0837-2016
Venlafaxine 75 mg Tablet, Compare to Effexor 75 mg Tablet, a) 30-count bottle (NDC 636290-3324-2), b) 100-count bottle (NDC 63629-3324-6),…
- FDA Drug
- Class III
- terminated
- Published 2016-05-11
On 2016-05-11 the FDA classified a Class III recall of Venlafaxine 75 mg Tablet, Compare to Effexor 75 mg Tablet, a) 30-count bottle (NDC 636290-3324-2), b) 100-count bottle (NDC 63629-3324-6),… by Bryant Ranch Prepack, citing labeling: Label Mix-Up: Bryant Ranch received Tevas venlafaxine hydrochloride extended-release tablets for repackaging, but labeled it incorrectly as the immediate release formula….
Read the official FDA Drug notice
| Agency | FDA Drug |
|---|---|
| Recall number | D-0837-2016 |
| Classification | Class III |
| Status | terminated |
| Initiated | 2016-03-25 |
| Published | 2016-05-11 |
| Last updated | 2026-09-13 11:51 UTC |
| Company | Bryant Ranch Prepack |
| Distribution | US |
Product
Venlafaxine 75 mg Tablet, Compare to Effexor 75 mg Tablet, a) 30-count bottle (NDC 636290-3324-2), b) 100-count bottle (NDC 63629-3324-6), Rx Only, Manufactured by Teva Pharmaceuticals USA, Inc. Packaged by Bryant Ranch.
Reason
Labeling: Label Mix-Up: Bryant Ranch received Tevas venlafaxine hydrochloride extended-release tablets for repackaging, but labeled it incorrectly as the immediate release formulation.
Identifiers
| ndc | 63629-3324-1 |
|---|---|
| ndc | 63629-3324-2 |
| ndc | 63629-3324-3 |
| ndc | 63629-3324-4 |
| ndc | 63629-3324-5 |
| ndc | 63629-3324-6 |
| ndc | 36290-3324-2 |
| code_info | Lot # 94983; Exp 10/17 |
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-0837-2016%22
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