venlafaxine

Product NDC

50090-2961

11-digit product format

500902961

Labeler code

50090

Product ID

50090-2961_33006850-a948-44cb-8506-b8de237e1d51

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

venlafaxine

Dosage form

TABLET

Route

ORAL

Labeler

A-S Medication Solutions

Application

ANDA078932

Marketing category

ANDA

Marketing start

2010-12-21

Marketing end

0000-00-00

Substance

VENLAFAXINE HYDROCHLORIDE

Active strength

75 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