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These highlights do not include all the information needed to use VENLAFAXINE HYDROCHLORIDE EXTENDED-RELEASE CAPSULES safely and effectively. See full prescribing information for VENLAFAXINE HYDROCHLORIDE EXTENDED-RELEASE CAPSULES. VENLAFAXINE HYDROCHLORIDE extended-release capsules, for oral use Initial U.S. Approval: 1997
Medication labelWhy this: Advisory · dailymed-prescription
Venlafaxine Hydrochloride Extended-Release Capsules, USP are indicated in adults for the treatment of: •Major Depressive Disorder (MDD) [see Clinical Studies (14.1)] •Generalized Anxiety Disorder (GAD) [see Clinical Studies (14.2)] •Social Anxiety Disorder (SAD) [see Clinical Studies (14.3)] •Panic Disorder (PD) [see Clinical Studies (14.4)]
- generic_name
- venlafaxine hydrochloride
- product_names
- Venlafaxine Hydrochloride
- ndc
- 68788-8682, 42806-601, 68788-8682-3, 68788-8682-6, 68788-8682-9, 68788-8682-1, 68788-8682-8
- group
- drugs
- license
- us-gov-pd
- attribution
- Courtesy of the National Library of Medicine
- reviewed
- 2026-09-18
- language
- en