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HydrALAZINE Hydrochloride - 60429-064-10 - (HydrALAZINE Hydrochloride)

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Drug Information of HydrALAZINE Hydrochloride

Product NDC: 60429-064
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: 60429-064
Labeler Name: Golden State Medical Supply, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA090255
Marketing Category: ANDA
Start Marketing Date: 20081215

Package Information of HydrALAZINE Hydrochloride

Package NDC: 60429-064-10
Package Description: 1000 TABLET in 1 BOTTLE (60429-064-10)

NDC Information of HydrALAZINE Hydrochloride

NDC Code 60429-064-10
Proprietary Name HydrALAZINE Hydrochloride
Package Description 1000 TABLET in 1 BOTTLE (60429-064-10)
Product NDC 60429-064
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name HydrALAZINE Hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20081215
Marketing Category Name ANDA
Labeler Name Golden State Medical Supply, 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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