Venlafaxine

Product NDC

63629-5117

11-digit product format

636295117

Labeler code

63629

Product ID

63629-5117_7e6cccb9-9485-4039-91a0-d08599f0b664

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Venlafaxine

Dosage form

TABLET

Route

ORAL

Labeler

Bryant Ranch Prepack

Application

ANDA078554

Marketing category

ANDA

Marketing start

2012-11-30

Marketing end

0000-00-00

Substance

VENLAFAXINE HYDROCHLORIDE

Active strength

50 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