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Clonidine Hydrochloride - 67253-264-50 - (Clonidine Hydrochloride)

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Drug Information of Clonidine Hydrochloride

Product NDC: 67253-264
Proprietary Name: Clonidine Hydrochloride
Non Proprietary Name: Clonidine Hydrochloride
Active Ingredient(s): .2    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: 67253-264
Labeler Name: DAVA Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA071784
Marketing Category: ANDA
Start Marketing Date: 19880405

Package Information of Clonidine Hydrochloride

Package NDC: 67253-264-50
Package Description: 500 TABLET in 1 BOTTLE (67253-264-50)

NDC Information of Clonidine Hydrochloride

NDC Code 67253-264-50
Proprietary Name Clonidine Hydrochloride
Package Description 500 TABLET in 1 BOTTLE (67253-264-50)
Product NDC 67253-264
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Clonidine Hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19880405
Marketing Category Name ANDA
Labeler Name DAVA Pharmaceuticals, Inc.
Substance Name CLONIDINE HYDROCHLORIDE
Strength Number .2
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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