Guanfacine

Product NDC

70518-0790

11-digit product format

705180790

Labeler code

70518

Product ID

70518-0790_8ec93da5-1c5e-1282-e053-2a95a90a7589

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

guanfacine Hydrochloride

Dosage form

TABLET

Route

ORAL

Labeler

REMEDYREPACK INC.

Application

ANDA074796

Marketing category

ANDA

Marketing start

2017-10-13

Marketing end

0000-00-00

Substance

GUANFACINE HYDROCHLORIDE

Active strength

2 mg/1

Pharmacologic classes

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

NDC exclude flag

No

Listing certified through

2020-12-31

Current FDA listing

Historical FDA.report record