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Clonidine Hydrochloride - 55154-0685-0 - (Clonidine Hydrochloride)

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Drug Information of Clonidine Hydrochloride

Product NDC: 55154-0685
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: 55154-0685
Labeler Name: Cardinal Health
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA070974
Marketing Category: ANDA
Start Marketing Date: 20061120

Package Information of Clonidine Hydrochloride

Package NDC: 55154-0685-0
Package Description: 10 BLISTER PACK in 1 BAG (55154-0685-0) > 1 TABLET in 1 BLISTER PACK

NDC Information of Clonidine Hydrochloride

NDC Code 55154-0685-0
Proprietary Name Clonidine Hydrochloride
Package Description 10 BLISTER PACK in 1 BAG (55154-0685-0) > 1 TABLET in 1 BLISTER PACK
Product NDC 55154-0685
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Clonidine Hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20061120
Marketing Category Name ANDA
Labeler Name Cardinal Health
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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