VENLAFAXINE HYDROCHLORIDE

Product NDC

68071-1579

11-digit product format

680711579

Labeler code

68071

Product ID

68071-1579_61570857-69e0-7051-e053-2a91aa0a9cc3

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

VENLAFAXINE HYDROCHLORIDE

Dosage form

CAPSULE, EXTENDED RELEASE

Route

ORAL

Labeler

NuCare Pharmaceuticals, Inc.

Application

ANDA090899

Marketing category

ANDA

Marketing start

2011-01-06

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