NDC 80425-0477 – Venlafaxine Hydrochloride

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

Human Prescription Drug

Product NDC80425-0477

Product details

Brand name
Venlafaxine Hydrochloride
Generic name
Venlafaxine hydrochloride
Labeler
Advanced Rx of Tennessee, LLC
Dosage form
Tablet, Extended Release
Route
Oral
Marketing category
NDA AUTHORIZED GENERIC · NDA022104
Marketed since
January 30, 2025
Listing expires
December 31, 2026
Pharmacologic class
Serotonin and Norepinephrine Reuptake Inhibitor

Active ingredients

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

Package NDC codes (3)

Package NDCDescriptionSince
80425-0477-130 TABLET, EXTENDED RELEASE in 1 BOTTLE (80425-0477-1)Jan 30, 2025
80425-0477-260 TABLET, EXTENDED RELEASE in 1 BOTTLE (80425-0477-2)Jan 30, 2025
80425-0477-390 TABLET, EXTENDED RELEASE in 1 BOTTLE (80425-0477-3)Jan 30, 2025

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