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Hydralazine Hydrochloride - 17478-934-01 - (Hydralazine Hydrochloride)

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Drug Information of Hydralazine Hydrochloride

Product NDC: 17478-934
Proprietary Name: Hydralazine Hydrochloride
Non Proprietary Name: Hydralazine Hydrochloride
Active Ingredient(s): 20    mg/mL & nbsp;   Hydralazine Hydrochloride
Administration Route(s): INTRAMUSCULAR; INTRAVENOUS
Dosage Form(s): INJECTION
Coding System: National Drug Codes(NDC)

Labeler Information of Hydralazine Hydrochloride

Product NDC: 17478-934
Labeler Name: Akorn, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040730
Marketing Category: ANDA
Start Marketing Date: 20090501

Package Information of Hydralazine Hydrochloride

Package NDC: 17478-934-01
Package Description: 10 VIAL, SINGLE-DOSE in 1 CARTON (17478-934-01) > 1 mL in 1 VIAL, SINGLE-DOSE

NDC Information of Hydralazine Hydrochloride

NDC Code 17478-934-01
Proprietary Name Hydralazine Hydrochloride
Package Description 10 VIAL, SINGLE-DOSE in 1 CARTON (17478-934-01) > 1 mL in 1 VIAL, SINGLE-DOSE
Product NDC 17478-934
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Hydralazine Hydrochloride
Dosage Form Name INJECTION
Route Name INTRAMUSCULAR; INTRAVENOUS
Start Marketing Date 20090501
Marketing Category Name ANDA
Labeler Name Akorn, Inc.
Substance Name HYDRALAZINE HYDROCHLORIDE
Strength Number 20
Strength Unit mg/mL
Pharmaceutical Classes Arteriolar Vasodilation [PE],Arteriolar Vasodilator [EPC]

Complete Information of Hydralazine Hydrochloride


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