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Clonidine Hydrochloride - 60760-027-30 - (Clonidine Hydrochloride)

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Drug Information of Clonidine Hydrochloride

Product NDC: 60760-027
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: 60760-027
Labeler Name: St Marys Medical Park Pharmacy
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA070974
Marketing Category: ANDA
Start Marketing Date: 20100301

Package Information of Clonidine Hydrochloride

Package NDC: 60760-027-30
Package Description: 30 TABLET in 1 BOTTLE, PLASTIC (60760-027-30)

NDC Information of Clonidine Hydrochloride

NDC Code 60760-027-30
Proprietary Name Clonidine Hydrochloride
Package Description 30 TABLET in 1 BOTTLE, PLASTIC (60760-027-30)
Product NDC 60760-027
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Clonidine Hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20100301
Marketing Category Name ANDA
Labeler Name St Marys Medical Park Pharmacy
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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