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Hydralazine Hydrochloride - 35356-944-90 - (Hydralazine Hydrochloride)

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Drug Information of Hydralazine Hydrochloride

Product NDC: 35356-944
Proprietary Name: Hydralazine Hydrochloride
Non Proprietary Name: Hydralazine Hydrochloride
Active Ingredient(s): 25    mg/1 & nbsp;   Hydralazine Hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Hydralazine Hydrochloride

Product NDC: 35356-944
Labeler Name: Lake Erie Medical DBA Quality Care Products LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA090527
Marketing Category: ANDA
Start Marketing Date: 20090601

Package Information of Hydralazine Hydrochloride

Package NDC: 35356-944-90
Package Description: 90 TABLET in 1 BOTTLE (35356-944-90)

NDC Information of Hydralazine Hydrochloride

NDC Code 35356-944-90
Proprietary Name Hydralazine Hydrochloride
Package Description 90 TABLET in 1 BOTTLE (35356-944-90)
Product NDC 35356-944
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Hydralazine Hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20090601
Marketing Category Name ANDA
Labeler Name Lake Erie Medical DBA Quality Care Products LLC
Substance Name HYDRALAZINE HYDROCHLORIDE
Strength Number 25
Strength Unit mg/1
Pharmaceutical Classes Arteriolar Vasodilation [PE],Arteriolar Vasodilator [EPC]

Complete Information of Hydralazine Hydrochloride


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