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NDC 65862-0697-05

Venlafaxine Hydrochloride 150 mg/1 CAPSULE, EXTENDED RELEASE

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NDC
65862-0697-05
Generic Name
Venlafaxine Hydrochloride
Brand Name
Venlafaxine Hydrochloride
Strength
150 mg/1
Dosage Form
CAPSULE, EXTENDED RELEASE
Route
ORAL
Package Size
Labeler
Aurobindo Pharma Limited

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 for the treatm…

Source: FDA. For professional use only. Not a substitute for prescribing information.

Other Venlafaxine Hydrochloride NDC Codes

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