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Clonidine Hydrochloride - 0615-2574-39 - (Clonidine Hydrochloride)

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Drug Information of Clonidine Hydrochloride

Product NDC: 0615-2574
Proprietary Name: Clonidine Hydrochloride
Non Proprietary Name: Clonidine Hydrochloride
Active Ingredient(s): .3    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: 0615-2574
Labeler Name: NCS HealthCare of KY, Inc dba Vangard Labs
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA070974
Marketing Category: ANDA
Start Marketing Date: 19950103

Package Information of Clonidine Hydrochloride

Package NDC: 0615-2574-39
Package Description: 30 TABLET in 1 BLISTER PACK (0615-2574-39)

NDC Information of Clonidine Hydrochloride

NDC Code 0615-2574-39
Proprietary Name Clonidine Hydrochloride
Package Description 30 TABLET in 1 BLISTER PACK (0615-2574-39)
Product NDC 0615-2574
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Clonidine Hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19950103
Marketing Category Name ANDA
Labeler Name NCS HealthCare of KY, Inc dba Vangard Labs
Substance Name CLONIDINE HYDROCHLORIDE
Strength Number .3
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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