Venlafaxine

Product NDC

0615-6566

11-digit product format

006156566

Labeler code

0615

Product ID

0615-6566_f116f679-6ab0-4aec-9837-01b9acbffba4

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Venlafaxine

Dosage form

TABLET

Route

ORAL

Labeler

NCS HealthCare of KY, Inc dba Vangard Labs

Application

ANDA077653

Marketing category

ANDA

Marketing start

2008-06-13

Marketing end

0000-00-00

Substance

VENLAFAXINE HYDROCHLORIDE

Active strength

38 mg/1

Pharmacologic classes

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

NDC exclude flag

E

Listing certified through

2017-12-31

Current FDA listing

Historical FDA.report record