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Hydralazine Hydrochloride - 55154-9367-5 - (HYDRALAZINE HYDROCHLORIDE)

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Drug Information of Hydralazine Hydrochloride

Product NDC: 55154-9367
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: 55154-9367
Labeler Name: Cardinal Health
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040388
Marketing Category: ANDA
Start Marketing Date: 20110131

Package Information of Hydralazine Hydrochloride

Package NDC: 55154-9367-5
Package Description: 5 VIAL, SINGLE-DOSE in 1 BAG (55154-9367-5) > 1 mL in 1 VIAL, SINGLE-DOSE

NDC Information of Hydralazine Hydrochloride

NDC Code 55154-9367-5
Proprietary Name Hydralazine Hydrochloride
Package Description 5 VIAL, SINGLE-DOSE in 1 BAG (55154-9367-5) > 1 mL in 1 VIAL, SINGLE-DOSE
Product NDC 55154-9367
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name HYDRALAZINE HYDROCHLORIDE
Dosage Form Name INJECTION
Route Name INTRAMUSCULAR; INTRAVENOUS
Start Marketing Date 20110131
Marketing Category Name ANDA
Labeler Name Cardinal Health
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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