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Hydralazine Hydrochloride - 52125-365-02 - (Hydralazine Hydrochloride)

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Drug Information of Hydralazine Hydrochloride

Product NDC: 52125-365
Proprietary Name: Hydralazine Hydrochloride
Non Proprietary Name: Hydralazine Hydrochloride
Active Ingredient(s): 25    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: 52125-365
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA090527
Marketing Category: ANDA
Start Marketing Date: 20130513

Package Information of Hydralazine Hydrochloride

Package NDC: 52125-365-02
Package Description: 30 TABLET in 1 BLISTER PACK (52125-365-02)

NDC Information of Hydralazine Hydrochloride

NDC Code 52125-365-02
Proprietary Name Hydralazine Hydrochloride
Package Description 30 TABLET in 1 BLISTER PACK (52125-365-02)
Product NDC 52125-365
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Hydralazine Hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20130513
Marketing Category Name ANDA
Labeler Name REMEDYREPACK INC.
Substance Name HYDRALAZINE HYDROCHLORIDE
Strength Number 25
Strength Unit mg/1
Pharmaceutical Classes Arteriolar Vasodilation [PE],Arteriolar Vasodilator [EPC]

Complete Information of Hydralazine Hydrochloride


General Information