Venlafaxine Hydrochloride

Product NDC

59762-0182

11-digit product format

597620182

Labeler code

59762

Product ID

59762-0182_efcd1626-4fc3-494a-bb29-05e2255d2c1c

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

VENLAFAXINE HYDROCHLORIDE

Dosage form

CAPSULE, EXTENDED RELEASE

Route

ORAL

Labeler

Greenstone LLC

Application

NDA020699

Marketing category

NDA AUTHORIZED GENERIC

Marketing start

2011-06-02

Marketing end

2019-05-31

Substance

VENLAFAXINE HYDROCHLORIDE

Active strength

150 mg/1

Pharmacologic classes

Norepinephrine Uptake Inhibitors [MoA],Serotonin and Norepinephrine Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA]

NDC exclude flag

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record