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NDC 70934-0571-30 HYDRALAZINE HYDROCHLORIDE 25 mg/1 Details

HYDRALAZINE HYDROCHLORIDE 25 mg/1

HYDRALAZINE HYDROCHLORIDE is a ORAL TABLET, FILM COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Denton Pharma, Inc. dba Northwind Pharmaceuticals. The primary component is HYDRALAZINE HYDROCHLORIDE.

MedlinePlus Drug Summary

Hydralazine is used to treat high blood pressure. Hydralazine is in a class of medications called vasodilators. It works by relaxing the blood vessels so that blood can flow more easily through the body. High blood pressure is a common condition and when not treated, can cause damage to the brain, heart, blood vessels, kidneys and other parts of the body. Damage to these organs may cause heart disease, a heart attack, heart failure, stroke, kidney failure, loss of vision, and other problems. In addition to taking medication, making lifestyle changes will also help to control your blood pressure. These changes include eating a diet that is low in fat and salt, maintaining a healthy weight, exercising at least 30 minutes most days, not smoking, and using alcohol in moderation.

Related Packages: 70934-0571-30
Last Updated: 12/01/2022
MedLinePlus Full Drug Details: Hydralazine

Product Information

NDC	70934-0571
Product ID	70934-571_f19ae5ec-7050-4029-e053-2a95a90a73fb
Associated GPIs
GCN Sequence Number	n/a
GCN Sequence Number Description	n/a
HIC3	n/a
HIC3 Description	n/a
GCN	n/a
HICL Sequence Number	n/a
HICL Sequence Number Description	n/a
Brand/Generic	n/a
Proprietary Name	HYDRALAZINE HYDROCHLORIDE
Proprietary Name Suffix	n/a
Non-Proprietary Name	hydralazine hydrochloride
Product Type	HUMAN PRESCRIPTION DRUG
Dosage Form	TABLET, FILM COATED
Route	ORAL
Active Ingredient Strength	25
Active Ingredient Units	mg/1
Substance Name	HYDRALAZINE HYDROCHLORIDE
Labeler Name	Denton Pharma, Inc. dba Northwind Pharmaceuticals
Pharmaceutical Class	Arteriolar Vasodilation [PE], Arteriolar Vasodilator [EPC]
DEA Schedule	n/a
Marketing Category	ANDA
Application Number	ANDA086242
Listing Certified Through	n/a

Package

NDC 70934-0571-30 (70934057130)

Pricing Information	N/A
NDC Package Code	70934-571-30
Billing NDC	70934057130
Package	30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70934-571-30)
Marketing Start Date	2020-02-26
NDC Exclude Flag	N