Guanfacine

Product NDC

0781-5456

11-digit product format

007815456

Labeler code

0781

Product ID

0781-5456_5a58b948-d0ce-4f3a-9c10-249c605efcc8

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

Guanfacine

Dosage form

TABLET, EXTENDED RELEASE

Route

ORAL

Labeler

Sandoz Inc

Application

ANDA202568

Marketing category

ANDA

Marketing start

2015-06-03

Marketing end

2019-12-31

Substance

GUANFACINE HYDROCHLORIDE

Active strength

3 mg/1

Pharmacologic classes

Central alpha-2 Adrenergic Agonist [EPC],Adrenergic alpha2-Agonists [MoA]

NDC exclude flag

No

Listing certified through

0000-00-00

Current FDA listing

Historical FDA.report record