Venlafaxine Hydrochloride

Product NDC

68071-4250

11-digit product format

680714250

Labeler code

68071

Product ID

68071-4250_888d620e-24eb-c476-e053-2a95a90a763c

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Venlafaxine Hydrochloride

Dosage form

CAPSULE, EXTENDED RELEASE

Route

ORAL

Labeler

NuCare Pharmaceuticals,Inc.

Application

ANDA076565

Marketing category

ANDA

Marketing start

2010-07-01

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

2020-12-31

Current FDA listing

Historical FDA.report record