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Hydralazine Hydrochloride - 63323-614-55 - (HYDRALAZINE HYDROCHLORIDE)

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Drug Information of Hydralazine Hydrochloride

Product NDC: 63323-614
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: 63323-614
Labeler Name: APP Pharmaceuticals, LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA040388
Marketing Category: ANDA
Start Marketing Date: 20010905

Package Information of Hydralazine Hydrochloride

Package NDC: 63323-614-55
Package Description: 25 VIAL, SINGLE-DOSE in 1 TRAY (63323-614-55) > 1 mL in 1 VIAL, SINGLE-DOSE

NDC Information of Hydralazine Hydrochloride

NDC Code 63323-614-55
Proprietary Name Hydralazine Hydrochloride
Package Description 25 VIAL, SINGLE-DOSE in 1 TRAY (63323-614-55) > 1 mL in 1 VIAL, SINGLE-DOSE
Product NDC 63323-614
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name HYDRALAZINE HYDROCHLORIDE
Dosage Form Name INJECTION
Route Name INTRAMUSCULAR; INTRAVENOUS
Start Marketing Date 20010905
Marketing Category Name ANDA
Labeler Name APP Pharmaceuticals, LLC
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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