NDC 47335-758 – Venlafaxine Hydrochloride

Venlafaxine Hydrochloride 150 mg/1 · Tablet, Extended Release · Oral

Human Prescription Drug

Product NDC47335-758

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
December 15, 2014
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
47335-758-08100 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-758-08)Dec 15, 2014
47335-758-181000 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-758-18)Dec 15, 2014
47335-758-8190 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-758-81)Dec 15, 2014
47335-758-8330 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-758-83)Dec 15, 2014
47335-758-88100 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-758-88)Dec 15, 2014
47335-758-992 BLISTER PACK in 1 BOX, UNIT-DOSE (47335-758-99) / 10 TABLET, EXTENDED RELEASE in 1 BLISTER PACKMar 29, 2019

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