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Hydralazine Hydrochloride - 54868-2893-4 - (Hydralazine Hydrochloride)

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Drug Information of Hydralazine Hydrochloride

Product NDC: 54868-2893
Proprietary Name: Hydralazine Hydrochloride
Non Proprietary Name: Hydralazine Hydrochloride
Active Ingredient(s): 50    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: 54868-2893
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA086242
Marketing Category: ANDA
Start Marketing Date: 20070917

Package Information of Hydralazine Hydrochloride

Package NDC: 54868-2893-4
Package Description: 270 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (54868-2893-4)

NDC Information of Hydralazine Hydrochloride

NDC Code 54868-2893-4
Proprietary Name Hydralazine Hydrochloride
Package Description 270 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (54868-2893-4)
Product NDC 54868-2893
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Hydralazine Hydrochloride
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20070917
Marketing Category Name ANDA
Labeler Name Physicians Total Care, Inc.
Substance Name HYDRALAZINE HYDROCHLORIDE
Strength Number 50
Strength Unit mg/1
Pharmaceutical Classes Arteriolar Vasodilation [PE],Arteriolar Vasodilator [EPC]

Complete Information of Hydralazine Hydrochloride


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