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Clonidine Hydrochloride - 52584-656-61 - (Clonidine Hydrochloride)

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Drug Information of Clonidine Hydrochloride

Product NDC: 52584-656
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: 52584-656
Labeler Name: General Injectables & Vaccines, Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA070974
Marketing Category: ANDA
Start Marketing Date: 20100301

Package Information of Clonidine Hydrochloride

Package NDC: 52584-656-61
Package Description: 1 BLISTER PACK in 1 BAG (52584-656-61) > 1 TABLET in 1 BLISTER PACK

NDC Information of Clonidine Hydrochloride

NDC Code 52584-656-61
Proprietary Name Clonidine Hydrochloride
Package Description 1 BLISTER PACK in 1 BAG (52584-656-61) > 1 TABLET in 1 BLISTER PACK
Product NDC 52584-656
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Clonidine Hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20100301
Marketing Category Name ANDA
Labeler Name General Injectables & Vaccines, Inc
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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