NDC 13811-712 – Venlafaxine Hydrochloride

Venlafaxine Hydrochloride 37.5 mg/1 · Tablet, Extended Release · Oral

Human Prescription Drug

Product NDC13811-712

Product details

Brand name
Venlafaxine Hydrochloride
Generic name
Venlafaxine hydrochloride
Labeler
Trigen Laboratories, LLC
Dosage form
Tablet, Extended Release
Route
Oral
Marketing category
NDA AUTHORIZED GENERIC · NDA022104
Marketed since
April 29, 2010
Marketing end
December 31, 2026
Pharmacologic class
Serotonin and Norepinephrine Reuptake Inhibitor

Active ingredients

Uses, dosage, side effects and warnings for Venlafaxine Hydrochloride →

Package NDC codes (2)

Package NDCDescriptionSince
13811-712-3030 TABLET, EXTENDED RELEASE in 1 BOTTLE (13811-712-30)Apr 29, 2010
13811-712-9090 TABLET, EXTENDED RELEASE in 1 BOTTLE (13811-712-90)Apr 29, 2010

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