NDC 47335-794 – Venlafaxine Hydrochloride

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

Human Prescription Drug

Product NDC47335-794

Product details

Brand name
Venlafaxine Hydrochloride
Generic name
Venlafaxine Hydrochloride
Labeler
Sun Pharmaceutical Industries, Inc.
Dosage form
Tablet, Extended Release
Route
Oral
Marketing category
ANDA · ANDA091272
Marketed since
February 15, 2019
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 (6)

Package NDCDescriptionSince
47335-794-08100 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-794-08)Feb 15, 2019
47335-794-13500 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-794-13)Feb 15, 2019
47335-794-8190 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-794-81)Aug 15, 2019
47335-794-8330 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-794-83)Feb 15, 2019
47335-794-88100 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-794-88)Feb 15, 2019
47335-794-995 BLISTER PACK in 1 BOX, UNIT-DOSE (47335-794-99) / 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACKFeb 15, 2019

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