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Clonidine Hydrochloride - 50436-3523-1 - (Clonidine Hydrochloride)

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Drug Information of Clonidine Hydrochloride

Product NDC: 50436-3523
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: 50436-3523
Labeler Name: Unit Dose Services
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA070974
Marketing Category: ANDA
Start Marketing Date: 19950103

Package Information of Clonidine Hydrochloride

Package NDC: 50436-3523-1
Package Description: 30 TABLET in 1 BOTTLE (50436-3523-1)

NDC Information of Clonidine Hydrochloride

NDC Code 50436-3523-1
Proprietary Name Clonidine Hydrochloride
Package Description 30 TABLET in 1 BOTTLE (50436-3523-1)
Product NDC 50436-3523
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 Unit Dose Services
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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