Clonidine Hydrochloride

Product NDC

70518-1837

11-digit product format

705181837

Labeler code

70518

Product ID

70518-1837_80c61f9e-9a8d-6a75-e053-2a91aa0a1834

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

clonidine hydrochloride

Dosage form

TABLET

Route

ORAL

Labeler

REMEDYREPACK INC.

Application

ANDA070317

Marketing category

ANDA

Marketing start

2019-01-30

Marketing end

0000-00-00

Substance

CLONIDINE HYDROCHLORIDE

Active strength

0 mg/1

Pharmacologic classes

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

NDC exclude flag

No

Listing certified through

2020-12-31

Current FDA listing

Historical FDA.report record