Clonidine Hydrochloride

Product NDC

68788-9535

11-digit product format

687889535

Labeler code

68788

Product ID

68788-9535_607062ea-31bd-4fd4-b223-cbed79f1bf44

Type

HUMAN PRESCRIPTION DRUG

Nonproprietary name

clonidine hydrochloride

Dosage form

TABLET

Route

ORAL

Labeler

Preferred Pharmaceuticals, Inc.

Application

ANDA077901

Marketing category

ANDA

Marketing start

2014-10-22

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

2019-12-31

Current FDA listing

Historical FDA.report record