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Hydralazine Hydrochloride - 49884-027-10 - (Hydralazine Hydrochloride)

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Drug Information of Hydralazine Hydrochloride

Product NDC: 49884-027
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: 49884-027
Labeler Name: Par Pharmaceutical, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA086961
Marketing Category: ANDA
Start Marketing Date: 19800227

Package Information of Hydralazine Hydrochloride

Package NDC: 49884-027-10
Package Description: 1000 TABLET in 1 BOTTLE (49884-027-10)

NDC Information of Hydralazine Hydrochloride

NDC Code 49884-027-10
Proprietary Name Hydralazine Hydrochloride
Package Description 1000 TABLET in 1 BOTTLE (49884-027-10)
Product NDC 49884-027
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 Par Pharmaceutical, Inc.
Substance Name HYDRALAZINE HYDROCHLORIDE
Strength Number 25
Strength Unit mg/1
Pharmaceutical Classes Arteriolar Vasodilation [PE],Arteriolar Vasodilator [EPC]

Complete Information of Hydralazine Hydrochloride


General Information