VENLAFAXINE HYDROCHLORIDE

Product NDC

0904-6246

11-digit product format

009046246

Labeler code

0904

Product ID

0904-6246_a13ec810-ee8c-456c-a62c-42d0a8641082

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

VENLAFAXINE HYDROCHLORIDE

Dosage form

CAPSULE, EXTENDED RELEASE

Route

ORAL

Labeler

Major Pharmaceuticals

Application

ANDA078865

Marketing category

ANDA

Marketing start

2011-06-07

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

No

Listing certified through

2019-12-31

Current FDA listing

Historical FDA.report record