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NDC 70934-0170-30 Hydrochlorothiazide 12.5 mg/1 Details

Hydrochlorothiazide 12.5 mg/1

Hydrochlorothiazide is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Denton Pharma, Inc. DBA Northwind Pharmaceuticals. The primary component is HYDROCHLOROTHIAZIDE.

MedlinePlus Drug Summary

Hydrochlorothiazide is used alone or in combination with other medications to treat high blood pressure. Hydrochlorothiazide is used to treat edema (fluid retention; excess fluid held in body tissues) caused by various medical problems, including heart, kidney, and liver disease and to treat edema caused by using certain medications including estrogen and corticosteroids. Hydrochlorothiazide is in a class of medications called diuretics ('water pills'). It works by causing the kidneys to get rid of unneeded water and salt from the body into the urine. 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: 70934-0170-30
Last Updated: 12/01/2022
MedLinePlus Full Drug Details: Hydrochlorothiazide

Product Information

NDC	70934-0170
Product ID	70934-170_d60a439a-b853-73af-e053-2995a90a207a
Associated GPIs	37600040000303
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	Hydrochlorothiazide
Proprietary Name Suffix	n/a
Non-Proprietary Name	Hydrochlorothiazide
Product Type	HUMAN PRESCRIPTION DRUG
Dosage Form	TABLET
Route	ORAL
Active Ingredient Strength	12.5
Active Ingredient Units	mg/1
Substance Name	HYDROCHLOROTHIAZIDE
Labeler Name	Denton Pharma, Inc. DBA Northwind Pharmaceuticals
Pharmaceutical Class	Increased Diuresis [PE], Thiazide Diuretic [EPC], Thiazides [CS]
DEA Schedule	n/a
Marketing Category	ANDA
Application Number	ANDA202556
Listing Certified Through	n/a

Package

NDC 70934-0170-30 (70934017030)

Pricing Information	N/A
NDC Package Code	70934-170-30
Billing NDC	70934017030
Package	30 TABLET in 1 BOTTLE, PLASTIC (70934-170-30)
Marketing Start Date	2018-09-19
NDC Exclude Flag	N