Venlafaxine 75 mg Tablet — Class III drug recall D-0837-2016
Terminated recall by Bryant Ranch Prepack Inc., reported 2016-05-11, distributed nationwide. Labeling: Label Mix-Up: Bryant Ranch received Tevas venlafaxine hydrochloride extended-release tablets for rep
| Recall number | D-0837-2016 |
|---|---|
| Product type | Drug |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Bryant Ranch Prepack Inc., Burbank, CA, United States |
| Recall initiated | 2016-03-25 |
| Classified | 2016-05-04 |
| Reported by FDA | 2016-05-11 |
| Terminated | 2016-08-29 |
| Distributed | Nationwide (US) |
| Reason classes | labeling |
| NDC | 36290-3324-02, 63629-3324, 63629-3324-01, 63629-3324-02, 63629-3324-03, 63629-3324-04, 63629-3324-05, 63629-3324-06 |
| Lot numbers | 10/17, 94983 |
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 for recall
Labeling: Label Mix-Up: Bryant Ranch received Tevas venlafaxine hydrochloride extended-release tablets for repackaging, but labeled it incorrectly as the immediate release formulation.
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-0837-2016. 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.