Recalls / Brands / Venlafaxine Hydrochloride
Venlafaxine Hydrochloride
4 FDA drug recalls involving brand “Venlafaxine Hydrochloride”.
| Date | Class | Product | Firm |
|---|---|---|---|
| 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, 150mg, packaged in a) 30-count bottles (NDC 68382-036-06), b) 90-count bottles | Zydus Pharmaceuticals 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 |