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CLONIDINE HYDROCHLORIDE - 35356-723-60 - (clonidine hydrochloride)

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Drug Information of CLONIDINE HYDROCHLORIDE

Product NDC: 35356-723
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: 35356-723
Labeler Name: Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA070925
Marketing Category: ANDA
Start Marketing Date: 19870904

Package Information of CLONIDINE HYDROCHLORIDE

Package NDC: 35356-723-60
Package Description: 60 TABLET in 1 BOTTLE (35356-723-60)

NDC Information of CLONIDINE HYDROCHLORIDE

NDC Code 35356-723-60
Proprietary Name CLONIDINE HYDROCHLORIDE
Package Description 60 TABLET in 1 BOTTLE (35356-723-60)
Product NDC 35356-723
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name clonidine hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19870904
Marketing Category Name ANDA
Labeler Name Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC
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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