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NDC 68788-8087-01 Hydralazine Hydrochloride 100 mg/1 Details

Hydralazine Hydrochloride 100 mg/1

Hydralazine Hydrochloride is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Preferred Pharmaceuticals, Inc.. 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: 68788-8087-01
Last Updated: 12/01/2022
MedLinePlus Full Drug Details: Hydralazine

Product Information

NDC	68788-8087
Product ID	68788-8087_9ab2b672-be92-4652-b711-48ff95cdb6d7
Associated GPIs	36400010100320
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
Route	ORAL
Active Ingredient Strength	100
Active Ingredient Units	mg/1
Substance Name	HYDRALAZINE HYDROCHLORIDE
Labeler Name	Preferred Pharmaceuticals, Inc.
Pharmaceutical Class	Arteriolar Vasodilation [PE], Arteriolar Vasodilator [EPC]
DEA Schedule	n/a
Marketing Category	ANDA
Application Number	ANDA040901
Listing Certified Through	2024-12-31

Package

NDC 68788-8087-01 (68788808701)

Pricing Information	N/A
NDC Package Code	68788-8087-1
Billing NDC	68788808701
Package	100 TABLET in 1 BOTTLE (68788-8087-1)
Marketing Start Date	2021-10-05
NDC Exclude Flag	N