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Hydralazine Hydrochloride - 54868-0536-2 - (Hydralazine Hydrochloride)

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Drug Information of Hydralazine Hydrochloride

Product NDC: 54868-0536
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: 54868-0536
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA086242
Marketing Category: ANDA
Start Marketing Date: 20070410

Package Information of Hydralazine Hydrochloride

Package NDC: 54868-0536-2
Package Description: 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (54868-0536-2)

NDC Information of Hydralazine Hydrochloride

NDC Code 54868-0536-2
Proprietary Name Hydralazine Hydrochloride
Package Description 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (54868-0536-2)
Product NDC 54868-0536
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Hydralazine Hydrochloride
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20070410
Marketing Category Name ANDA
Labeler Name Physicians Total Care, 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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