Search by Drug Name or NDC

NDC 68788-7019-09 Spironolactone 100 mg/1 Details

Spironolactone 100 mg/1

Spironolactone is a ORAL TABLET, FILM COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Preferred Pharmaceuticals Inc.. The primary component is SPIRONOLACTONE.

MedlinePlus Drug Summary

Spironolactone is used to treat certain patients with hyperaldosteronism (the body produces too much aldosterone, a naturally occurring hormone); low potassium levels; heart failure; and in patients with edema (fluid retention) caused by various conditions, including liver, or kidney disease. It is also used alone or with other medications to treat high blood pressure. Spironolactone is in a class of medications called aldosterone receptor antagonists. It causes the kidneys to eliminate unneeded water and sodium from the body into the urine but reduces the loss of potassium from 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: 68788-7019-09
Last Updated: 12/01/2022
MedLinePlus Full Drug Details: Spironolactone

Product Information

NDC	68788-7019
Product ID	68788-7019_e0766e29-c69c-48b8-9801-a5565697c2b6
Associated GPIs	37500020000315
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	Spironolactone
Proprietary Name Suffix	n/a
Non-Proprietary Name	spironolactone
Product Type	HUMAN PRESCRIPTION DRUG
Dosage Form	TABLET, FILM COATED
Route	ORAL
Active Ingredient Strength	100
Active Ingredient Units	mg/1
Substance Name	SPIRONOLACTONE
Labeler Name	Preferred Pharmaceuticals Inc.
Pharmaceutical Class	Aldosterone Antagonist [EPC], Aldosterone Antagonists [MoA]
DEA Schedule	n/a
Marketing Category	ANDA
Application Number	ANDA203512
Listing Certified Through	2024-12-31

Package

NDC 68788-7019-09 (68788701909)

Pricing Information	N/A
NDC Package Code	68788-7019-9
Billing NDC	68788701909
Package	90 TABLET, FILM COATED in 1 BOTTLE (68788-7019-9)
Marketing Start Date	2017-10-11
NDC Exclude Flag	N