Drugplain

NDC 69367-418-30

Venlafaxine Hydrochloride 225 mg/1

Venlafaxine Hydrochloride · TABLET, EXTENDED RELEASE

No Recall History

Venlafaxine hydrochloride is an antidepressant medication taken by mouth as an extended-release tablet that is used to treat depression, anxiety disorders, and panic disorder. Your doctor will determine the appropriate dose for your condition.

Key Facts

Brand Name
Venlafaxine Hydrochloride
Generic Name
Venlafaxine Hydrochloride
NDC Code (Package)
69367-418-30
NDC Code (Product)
69367-418
Manufacturer
Westminster Pharmaceuticals, LLC
Strength
225 mg/1
Dosage Form
TABLET, EXTENDED RELEASE
Route
ORAL
Marketing Status
Application #
ANDA205468
Marketing Start
11/18/2025

Recall History

No Recall History

Not medical advice. This information is for reference only. Always consult your doctor or pharmacist.