NDC 70010-0184-03
Venlafaxine Hydrochloride 37.5 mg/1 CAPSULE, EXTENDED RELEASE
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NDC
70010-0184-03
Generic Name
Venlafaxine Hydrochloride
Brand Name
Venlafaxine Hydrochloride
Strength
37.5 mg/1
Dosage Form
CAPSULE, EXTENDED RELEASE
Route
ORAL
Package Size
—
Labeler
Granules Pharmaceuticals Inc.
FDA Drug Information
Indications & Usage
1 INDICATIONS AND USAGE Venlafaxine hydrochloride extended-release capsules 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) ] Venlafaxine hydrochloride extended-release capsules are a serotonin and norepinephrine reuptake inhibitor (SNRI) indicated fo…
Source: FDA. For professional use only. Not a substitute for prescribing information.
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