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Hydralazine Hydrochloride - 0615-0531-39 - (Hydralazine Hydrochloride)

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Drug Information of Hydralazine Hydrochloride

Product NDC: 0615-0531
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: 0615-0531
Labeler Name: NCS HealthCare of KY, Inc dba Vangard Labs
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA086961
Marketing Category: ANDA
Start Marketing Date: 19800227

Package Information of Hydralazine Hydrochloride

Package NDC: 0615-0531-39
Package Description: 30 TABLET in 1 BLISTER PACK (0615-0531-39)

NDC Information of Hydralazine Hydrochloride

NDC Code 0615-0531-39
Proprietary Name Hydralazine Hydrochloride
Package Description 30 TABLET in 1 BLISTER PACK (0615-0531-39)
Product NDC 0615-0531
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Hydralazine Hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19800227
Marketing Category Name ANDA
Labeler Name NCS HealthCare of KY, Inc dba Vangard Labs
Substance Name HYDRALAZINE HYDROCHLORIDE
Strength Number 25
Strength Unit mg/1
Pharmaceutical Classes Arteriolar Vasodilation [PE],Arteriolar Vasodilator [EPC]

Complete Information of Hydralazine Hydrochloride


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