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Hydralazine Hydrochloride - 23155-004-10 - (Hydralazine Hydrochloride)

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Drug Information of Hydralazine Hydrochloride

Product NDC: 23155-004
Proprietary Name: Hydralazine Hydrochloride
Non Proprietary Name: Hydralazine Hydrochloride
Active Ingredient(s): 100    mg/1 & nbsp;   Hydralazine Hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Hydralazine Hydrochloride

Product NDC: 23155-004
Labeler Name: Heritage Pharmaceuticals Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA086242
Marketing Category: ANDA
Start Marketing Date: 20070406

Package Information of Hydralazine Hydrochloride

Package NDC: 23155-004-10
Package Description: 1000 TABLET, FILM COATED in 1 BOTTLE (23155-004-10)

NDC Information of Hydralazine Hydrochloride

NDC Code 23155-004-10
Proprietary Name Hydralazine Hydrochloride
Package Description 1000 TABLET, FILM COATED in 1 BOTTLE (23155-004-10)
Product NDC 23155-004
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Hydralazine Hydrochloride
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20070406
Marketing Category Name ANDA
Labeler Name Heritage Pharmaceuticals Inc
Substance Name HYDRALAZINE HYDROCHLORIDE
Strength Number 100
Strength Unit mg/1
Pharmaceutical Classes Arteriolar Vasodilation [PE],Arteriolar Vasodilator [EPC]

Complete Information of Hydralazine Hydrochloride


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