Recalls / Active ingredient / Venlafaxine Hydrochloride

Venlafaxine Hydrochloride

9 FDA drug recalls involving the active ingredient “Venlafaxine Hydrochloride” — 1 Class I.

Date	Class	Product	Firm
2025-03-21	Class II	Venlafaxine Tablets, USP, 75 mg, 100 Tablets, Rx only, Mfg. by: Zydus Lifesciences Ltd, Ahmedabad, India, Dist	Zydus Pharmaceuticals (USA) Inc
2025-01-16	Class III	Venlafaxine Extended-Release Tablets, 150mg, Rx only, 90 Tablets, Manufactured by Appco Pharma. LLC, NDC 43598	Appco Pharma LLC
2024-06-21	Class II	Venlafaxine Hydrochloride Extended-Release Capsules, USP 37.5mg, packaged in a) 90-count bottles (NDC 68382-03	Zydus Pharmaceuticals (USA) Inc
2016-12-22	Class II	Venlafaxine Hydrochloride extended release capsules, 37.5 mg, 30-count bottles, Rx Only, Manufactured for: Aur	Aurobindo Pharma USA Inc
2016-07-19	Class II	Venlafaxine HCL ER Capsule USP, 75mg, packaged in a) 30-count bottles (NDC 68382-035-06), b) 90-count bottles	Zydus Pharmaceuticals USA Inc
2016-07-19	Class II	Venlafaxine HCL ER Capsule USP, 150mg, packaged in a) 30-count bottles (NDC 68382-036-06), b) 90-count bottles	Zydus Pharmaceuticals USA Inc
2016-03-25	Class III	Venlafaxine 75 mg Tablet, Compare to Effexor 75 mg Tablet, a) 30-count bottle (NDC 636290-3324-2), b) 100-coun	Bryant Ranch Prepack Inc.
2014-03-06	Class I	Effexor XR (venlafaxine HCl) Extended-Release Capsules, 150 mg, packaged in a) 30-count Unit of Use bottles (N	Pfizer Us Pharmaceutical Group
2013-03-05	Class II	Venlafaxine Hydrochloride Tablets, 75 mg*, 100-count tablets per bottle, Rx only, Manufactured by: Cadila Heal	Zydus Pharmaceuticals USA Inc