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Hydralazine Hydrochloride - 68084-520-21 - (Hydralazine Hydrochloride)

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Drug Information of Hydralazine Hydrochloride

Product NDC: 68084-520
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
Coding System: National Drug Codes(NDC)

Labeler Information of Hydralazine Hydrochloride

Product NDC: 68084-520
Labeler Name: AMERISOURCEBERGEN DRUG CORPORATION
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA086242
Marketing Category: ANDA
Start Marketing Date: 20110919

Package Information of Hydralazine Hydrochloride

Package NDC: 68084-520-21
Package Description: 3 BLISTER PACK in 1 CARTON (68084-520-21) > 10 TABLET in 1 BLISTER PACK (68084-520-11)

NDC Information of Hydralazine Hydrochloride

NDC Code 68084-520-21
Proprietary Name Hydralazine Hydrochloride
Package Description 3 BLISTER PACK in 1 CARTON (68084-520-21) > 10 TABLET in 1 BLISTER PACK (68084-520-11)
Product NDC 68084-520
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Hydralazine Hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20110919
Marketing Category Name ANDA
Labeler Name AMERISOURCEBERGEN DRUG CORPORATION
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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