Home > National Drug Code (NDC) > HYDRALAZINE HYDROCHLORIDE

HYDRALAZINE HYDROCHLORIDE - 49349-079-02 - (HYDRALAZINE HYDROCHLORIDE)

Alphabetical Index


Drug Information of HYDRALAZINE HYDROCHLORIDE

Product NDC: 49349-079
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: 49349-079
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA088467
Marketing Category: ANDA
Start Marketing Date: 20101118

Package Information of HYDRALAZINE HYDROCHLORIDE

Package NDC: 49349-079-02
Package Description: 30 TABLET in 1 BLISTER PACK (49349-079-02)

NDC Information of HYDRALAZINE HYDROCHLORIDE

NDC Code 49349-079-02
Proprietary Name HYDRALAZINE HYDROCHLORIDE
Package Description 30 TABLET in 1 BLISTER PACK (49349-079-02)
Product NDC 49349-079
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name HYDRALAZINE HYDROCHLORIDE
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20101118
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