Search by Drug Name or NDC

NDC 68788-8928-09 Hydrochlorothiazide 50 mg/1 Details

Hydrochlorothiazide 50 mg/1

Hydrochlorothiazide is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Preferred Pharmaceuticals Inc.. 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: 68788-8928-09
Last Updated: 12/01/2022
MedLinePlus Full Drug Details: Hydrochlorothiazide

Product Information

NDC	68788-8928
Product ID	68788-8928_c9f881b6-bb6f-4248-808d-127c21ccee0c
Associated GPIs	37600040000310
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	50
Active Ingredient Units	mg/1
Substance Name	HYDROCHLOROTHIAZIDE
Labeler Name	Preferred Pharmaceuticals Inc.
Pharmaceutical Class	Increased Diuresis [PE], Thiazide Diuretic [EPC], Thiazides [CS]
DEA Schedule	n/a
Marketing Category	ANDA
Application Number	ANDA202556
Listing Certified Through	2022-12-31

Package

NDC 68788-8928-09 (68788892809)

Pricing Information	N/A
NDC Package Code	68788-8928-9
Billing NDC	68788892809
Package	90 TABLET in 1 BOTTLE (68788-8928-9)
Marketing Start Date	2015-10-07
NDC Exclude Flag	N