Venlafaxine Hydrochloride

Product NDC

50090-1214

11-digit product format

500901214

Labeler code

50090

Product ID

50090-1214_e63d5134-b14c-4634-8a49-1537dfc2c2e5

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Venlafaxine Hydrochloride

Dosage form

CAPSULE, EXTENDED RELEASE

Route

ORAL

Labeler

A-S Medication Solutions

Application

ANDA076565

Marketing category

ANDA

Marketing start

2010-07-01

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