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HYDRALAZINE HYDROCHLORIDE - 21695-679-90 - (Hydralazine Hydrochloride)

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Drug Information of HYDRALAZINE HYDROCHLORIDE

Product NDC: 21695-679
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: 21695-679
Labeler Name: Rebel Distributors Corp
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040901
Marketing Category: ANDA
Start Marketing Date: 20080912

Package Information of HYDRALAZINE HYDROCHLORIDE

Package NDC: 21695-679-90
Package Description: 90 TABLET in 1 BOTTLE (21695-679-90)

NDC Information of HYDRALAZINE HYDROCHLORIDE

NDC Code 21695-679-90
Proprietary Name HYDRALAZINE HYDROCHLORIDE
Package Description 90 TABLET in 1 BOTTLE (21695-679-90)
Product NDC 21695-679
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Hydralazine Hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20080912
Marketing Category Name ANDA
Labeler Name Rebel Distributors Corp
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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