Guanfacine

Product NDC

70518-0268

11-digit product format

705180268

Labeler code

70518

Product ID

70518-0268_9ffe03d6-8d69-5f61-e053-2995a90a0b61

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

guanfacine Hydrochloride

Dosage form

TABLET

Route

ORAL

Labeler

REMEDYREPACK INC.

Application

ANDA074796

Marketing category

ANDA

Marketing start

2017-03-01

Marketing end

0000-00-00

Substance

GUANFACINE HYDROCHLORIDE

Active strength

1 mg/1

Pharmacologic classes

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

NDC exclude flag

No

Listing certified through

2021-12-31

Current FDA listing

Historical FDA.report record