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Hydralazine Hydrochloride - 52584-901-25 - (Hydralazine Hydrochloride)

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Drug Information of Hydralazine Hydrochloride

Product NDC: 52584-901
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, SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Hydralazine Hydrochloride

Product NDC: 52584-901
Labeler Name: General Injectables & Vaccines, Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040136
Marketing Category: ANDA
Start Marketing Date: 20100801

Package Information of Hydralazine Hydrochloride

Package NDC: 52584-901-25
Package Description: 1 VIAL, SINGLE-DOSE in 1 BAG (52584-901-25) > 1 mL in 1 VIAL, SINGLE-DOSE

NDC Information of Hydralazine Hydrochloride

NDC Code 52584-901-25
Proprietary Name Hydralazine Hydrochloride
Package Description 1 VIAL, SINGLE-DOSE in 1 BAG (52584-901-25) > 1 mL in 1 VIAL, SINGLE-DOSE
Product NDC 52584-901
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Hydralazine Hydrochloride
Dosage Form Name INJECTION, SOLUTION
Route Name INTRAMUSCULAR; INTRAVENOUS
Start Marketing Date 20100801
Marketing Category Name ANDA
Labeler Name General Injectables & Vaccines, 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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