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Hydralazine Hydrochloride - 31722-521-01 - (Hydralazine Hydrochloride)

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Drug Information of Hydralazine Hydrochloride

Product NDC: 31722-521
Proprietary Name: Hydralazine Hydrochloride
Non Proprietary Name: Hydralazine Hydrochloride
Active Ingredient(s): 50    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: 31722-521
Labeler Name: Camber Pharmaceuticals
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040901
Marketing Category: ANDA
Start Marketing Date: 20100101

Package Information of Hydralazine Hydrochloride

Package NDC: 31722-521-01
Package Description: 12 BOTTLE in 1 CASE (31722-521-01) > 100 TABLET in 1 BOTTLE

NDC Information of Hydralazine Hydrochloride

NDC Code 31722-521-01
Proprietary Name Hydralazine Hydrochloride
Package Description 12 BOTTLE in 1 CASE (31722-521-01) > 100 TABLET in 1 BOTTLE
Product NDC 31722-521
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Hydralazine Hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20100101
Marketing Category Name ANDA
Labeler Name Camber Pharmaceuticals
Substance Name HYDRALAZINE HYDROCHLORIDE
Strength Number 50
Strength Unit mg/1
Pharmaceutical Classes Arteriolar Vasodilation [PE],Arteriolar Vasodilator [EPC]

Complete Information of Hydralazine Hydrochloride


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