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Hydralazine Hydrochloride - 51079-074-20 - (Hydralazine Hydrochloride)

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Drug Information of Hydralazine Hydrochloride

Product NDC: 51079-074
Proprietary Name: Hydralazine Hydrochloride
Non Proprietary Name: Hydralazine Hydrochloride
Active Ingredient(s): 10    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: 51079-074
Labeler Name: UDL Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA089097
Marketing Category: ANDA
Start Marketing Date: 20110513

Package Information of Hydralazine Hydrochloride

Package NDC: 51079-074-20
Package Description: 100 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-074-20) > 1 TABLET in 1 BLISTER PACK (51079-074-01)

NDC Information of Hydralazine Hydrochloride

NDC Code 51079-074-20
Proprietary Name Hydralazine Hydrochloride
Package Description 100 BLISTER PACK in 1 BOX, UNIT-DOSE (51079-074-20) > 1 TABLET in 1 BLISTER PACK (51079-074-01)
Product NDC 51079-074
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Hydralazine Hydrochloride
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20110513
Marketing Category Name ANDA
Labeler Name UDL Laboratories, Inc.
Substance Name HYDRALAZINE HYDROCHLORIDE
Strength Number 10
Strength Unit mg/1
Pharmaceutical Classes Arteriolar Vasodilation [PE],Arteriolar Vasodilator [EPC]

Complete Information of Hydralazine Hydrochloride


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