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Clonidine Hydrochloride - 52125-171-02 - (clonidine hydrochloride)

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Drug Information of Clonidine Hydrochloride

Product NDC: 52125-171
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: 52125-171
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA070317
Marketing Category: ANDA
Start Marketing Date: 20130318

Package Information of Clonidine Hydrochloride

Package NDC: 52125-171-02
Package Description: 30 TABLET in 1 BLISTER PACK (52125-171-02)

NDC Information of Clonidine Hydrochloride

NDC Code 52125-171-02
Proprietary Name Clonidine Hydrochloride
Package Description 30 TABLET in 1 BLISTER PACK (52125-171-02)
Product NDC 52125-171
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name clonidine hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20130318
Marketing Category Name ANDA
Labeler Name REMEDYREPACK 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


General Information