NDC 31722-126 – Venlafaxine Hydrochloride

Venlafaxine Hydrochloride 225 mg/1 · Tablet, Extended Release · Oral

Human Prescription Drug

Product NDC31722-126

Product details

Brand name
Venlafaxine Hydrochloride
Generic name
Venlafaxine
Labeler
Camber Pharmaceuticals, Inc.
Dosage form
Tablet, Extended Release
Route
Oral
Marketing category
ANDA · ANDA214419
Marketed since
October 23, 2020
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 (2)

Package NDCDescriptionSince
31722-126-3030 TABLET, EXTENDED RELEASE in 1 BOTTLE (31722-126-30)Oct 23, 2020
31722-126-9090 TABLET, EXTENDED RELEASE in 1 BOTTLE (31722-126-90)Oct 23, 2020

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