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Clonidine Hydrochloride - 67046-098-30 - (Clonidine Hydrochloride)

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Drug Information of Clonidine Hydrochloride

Product NDC: 67046-098
Proprietary Name: Clonidine Hydrochloride
Non Proprietary Name: Clonidine Hydrochloride
Active Ingredient(s): .2    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: 67046-098
Labeler Name: Contract Pharmacy Services-PA
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA070317
Marketing Category: ANDA
Start Marketing Date: 20100729

Package Information of Clonidine Hydrochloride

Package NDC: 67046-098-30
Package Description: 30 TABLET in 1 BLISTER PACK (67046-098-30)

NDC Information of Clonidine Hydrochloride

NDC Code 67046-098-30
Proprietary Name Clonidine Hydrochloride
Package Description 30 TABLET in 1 BLISTER PACK (67046-098-30)
Product NDC 67046-098
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Clonidine Hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20100729
Marketing Category Name ANDA
Labeler Name Contract Pharmacy Services-PA
Substance Name CLONIDINE HYDROCHLORIDE
Strength Number .2
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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