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Hydralazine Hydrochloride - 24236-558-20 - (Hydralazine Hydrochloride)

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Drug Information of Hydralazine Hydrochloride

Product NDC: 24236-558
Proprietary Name: Hydralazine Hydrochloride
Non Proprietary Name: Hydralazine Hydrochloride
Active Ingredient(s): 10    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: 24236-558
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA089097
Marketing Category: ANDA
Start Marketing Date: 20130318

Package Information of Hydralazine Hydrochloride

Package NDC: 24236-558-20
Package Description: 100 TABLET in 1 CANISTER (24236-558-20)

NDC Information of Hydralazine Hydrochloride

NDC Code 24236-558-20
Proprietary Name Hydralazine Hydrochloride
Package Description 100 TABLET in 1 CANISTER (24236-558-20)
Product NDC 24236-558
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Hydralazine Hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20130318
Marketing Category Name ANDA
Labeler Name REMEDYREPACK INC.
Substance Name HYDRALAZINE HYDROCHLORIDE
Strength Number 10
Strength Unit mg/1
Pharmaceutical Classes Arteriolar Vasodilation [PE],Arteriolar Vasodilator [EPC]

Complete Information of Hydralazine Hydrochloride


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