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CLONIDINE HYDROCHLORIDE - 53489-217-01 - (clonidine hydrochloride)

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Drug Information of CLONIDINE HYDROCHLORIDE

Product NDC: 53489-217
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: 53489-217
Labeler Name: Mutual Pharmaceutical Company, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA070923
Marketing Category: ANDA
Start Marketing Date: 19870904

Package Information of CLONIDINE HYDROCHLORIDE

Package NDC: 53489-217-01
Package Description: 100 TABLET in 1 BOTTLE, PLASTIC (53489-217-01)

NDC Information of CLONIDINE HYDROCHLORIDE

NDC Code 53489-217-01
Proprietary Name CLONIDINE HYDROCHLORIDE
Package Description 100 TABLET in 1 BOTTLE, PLASTIC (53489-217-01)
Product NDC 53489-217
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 Mutual Pharmaceutical Company, Inc.
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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