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Clonidine Hydrochloride - 63739-060-10 - (Clonidine Hydrochloride)

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Drug Information of Clonidine Hydrochloride

Product NDC: 63739-060
Proprietary Name: Clonidine Hydrochloride
Non Proprietary Name: Clonidine Hydrochloride
Active Ingredient(s): .1    mg/1 & nbsp;   Clonidine Hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Clonidine Hydrochloride

Product NDC: 63739-060
Labeler Name: McKesson Packaging Services Business Unit of McKesson Corporation
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA070974
Marketing Category: ANDA
Start Marketing Date: 20070607

Package Information of Clonidine Hydrochloride

Package NDC: 63739-060-10
Package Description: 10 BLISTER PACK in 1 BOX, UNIT-DOSE (63739-060-10) > 10 TABLET in 1 BLISTER PACK

NDC Information of Clonidine Hydrochloride

NDC Code 63739-060-10
Proprietary Name Clonidine Hydrochloride
Package Description 10 BLISTER PACK in 1 BOX, UNIT-DOSE (63739-060-10) > 10 TABLET in 1 BLISTER PACK
Product NDC 63739-060
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Clonidine Hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20070607
Marketing Category Name ANDA
Labeler Name McKesson Packaging Services Business Unit of McKesson Corporation
Substance Name CLONIDINE HYDROCHLORIDE
Strength Number .1
Strength Unit mg/1
Pharmaceutical Classes Adrenergic alpha2-Agonists [MoA],Central alpha-2 Adrenergic Agonist [EPC]

Complete Information of Clonidine Hydrochloride


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