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NDC 68788-6784-09 Furosemide 40 mg/1 Details

Furosemide 40 mg/1

Furosemide is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Preferred Pharmaceuticals, Inc.. The primary component is FUROSEMIDE.

MedlinePlus Drug Summary

Furosemide is used alone or in combination with other medications to treat high blood pressure. Furosemide is used to treat edema (fluid retention; excess fluid held in body tissues) caused by various medical problems, including heart, kidney, and liver disease. Furosemide 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: 68788-6784-09
Last Updated: 12/01/2022
MedLinePlus Full Drug Details: Furosemide

Product Information

NDC	68788-6784
Product ID	68788-6784_7150b756-c8b2-4962-ac95-3faeaf1f9c9c
Associated GPIs	37200030000310
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	Furosemide
Proprietary Name Suffix	n/a
Non-Proprietary Name	Furosemide
Product Type	HUMAN PRESCRIPTION DRUG
Dosage Form	TABLET
Route	ORAL
Active Ingredient Strength	40
Active Ingredient Units	mg/1
Substance Name	FUROSEMIDE
Labeler Name	Preferred Pharmaceuticals, Inc.
Pharmaceutical Class	Increased Diuresis at Loop of Henle [PE], Loop Diuretic [EPC]
DEA Schedule	n/a
Marketing Category	ANDA
Application Number	ANDA077293
Listing Certified Through	2024-12-31

Package

NDC 68788-6784-09 (68788678409)

Pricing Information	N/A
NDC Package Code	68788-6784-9
Billing NDC	68788678409
Package	90 TABLET in 1 BOTTLE (68788-6784-9)
Marketing Start Date	2016-10-25
NDC Exclude Flag	N