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NDC 00574-0292-01 amiloride hydrochloride 5 mg/1 Details
amiloride hydrochloride 5 mg/1
amiloride hydrochloride is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Padagis US LLC. The primary component is AMILORIDE HYDROCHLORIDE.
MedlinePlus Drug Summary
Amiloride is usually used in combination with other diuretics ('water pills') to treat high blood pressure and heart failure in patients who have low amounts of potassium in their bodies or for whom low potassium levels in the body could be dangerous. Amiloride is in a class of medications called diuretics. It works by causing the kidneys to get rid of unneeded water and salt from the body into the urine, but reduces the loss of potassium. High blood pressure is a common condition, and when not treated it 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: 00574-0292-01Last Updated: 11/30/2022
MedLinePlus Full Drug Details: Amiloride
Product Information
NDC | 00574-0292 |
---|---|
Product ID | 0574-0292_8fcb7492-3943-4a51-ba0d-81a37c4bd04d |
Associated GPIs | 37500010100305 |
GCN Sequence Number | 008227 |
GCN Sequence Number Description | amiloride HCl TABLET 5 MG ORAL |
HIC3 | R1H |
HIC3 Description | POTASSIUM SPARING DIURETICS |
GCN | 27700 |
HICL Sequence Number | 003667 |
HICL Sequence Number Description | AMILORIDE HCL |
Brand/Generic | Generic |
Proprietary Name | amiloride hydrochloride |
Proprietary Name Suffix | n/a |
Non-Proprietary Name | amiloride hydrochloride |
Product Type | HUMAN PRESCRIPTION DRUG |
Dosage Form | TABLET |
Route | ORAL |
Active Ingredient Strength | 5 |
Active Ingredient Units | mg/1 |
Substance Name | AMILORIDE HYDROCHLORIDE |
Labeler Name | Padagis US LLC |
Pharmaceutical Class | Decreased Renal K+ Excretion [PE], Increased Diuresis [PE], Potassium-sparing Diuretic [EPC] |
DEA Schedule | n/a |
Marketing Category | NDA AUTHORIZED GENERIC |
Application Number | NDA018200 |
Listing Certified Through | 2024-12-31 |
Package
NDC 00574-0292-01 (00574029201)
NDC Package Code | 0574-0292-01 |
---|---|
Billing NDC | 00574029201 |
Package | 100 TABLET in 1 BOTTLE (0574-0292-01) |
Marketing Start Date | 2009-04-06 |
NDC Exclude Flag | N |
Pricing Information | |
Price Per Unit | 0.18216 |
Pricing Unit | EA |
Effective Date | 2024-02-21 |
NDC Description | AMILORIDE HCL 5 MG TABLET |
Pharmacy Type Indicator | C/I |
OTC | N |
Explanation Code | 1, 6 |
Classification for Rate Setting | G |
As of Date | 2024-02-21 |