Search by Drug Name or NDC
NDC 50090-0513-00 Amiloride Hydrochloride and Hydrochlorothiazide 5; 50 mg/1; mg/1 Details
Amiloride Hydrochloride and Hydrochlorothiazide 5; 50 mg/1; mg/1
Amiloride Hydrochloride and Hydrochlorothiazide is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by A-S Medication Solutions. The primary component is AMILORIDE HYDROCHLORIDE; HYDROCHLOROTHIAZIDE.
MedlinePlus Drug Summary
The combination of amiloride and hydrochlorothiazide is used alone or in combination with other medications 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 and hydrochlorothiazide are in a class of medications called diuretics ('water pills'). They work 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: 50090-0513-00Last Updated: 11/30/2022
MedLinePlus Full Drug Details: Amiloride and Hydrochlorothiazide
Product Information
| NDC | 50090-0513 |
|---|---|
| Product ID | 50090-0513_11f19f1c-770b-4f2c-ad26-df56013babce |
| Associated GPIs | 37990002100310 |
| GCN Sequence Number | 008178 |
| GCN Sequence Number Description | amiloride/hydrochlorothiazide TABLET 5 MG-50 MG ORAL |
| HIC3 | R1L |
| HIC3 Description | POTASSIUM SPARING DIURETICS IN COMBINATION |
| GCN | 82341 |
| HICL Sequence Number | 003648 |
| HICL Sequence Number Description | AMILORIDE HCL/HYDROCHLOROTHIAZIDE |
| Brand/Generic | Generic |
| Proprietary Name | Amiloride Hydrochloride and Hydrochlorothiazide |
| Proprietary Name Suffix | n/a |
| Non-Proprietary Name | Amiloride Hydrochloride and Hydrochlorothiazide |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Dosage Form | TABLET |
| Route | ORAL |
| Active Ingredient Strength | 5; 50 |
| Active Ingredient Units | mg/1; mg/1 |
| Substance Name | AMILORIDE HYDROCHLORIDE; HYDROCHLOROTHIAZIDE |
| Labeler Name | A-S Medication Solutions |
| Pharmaceutical Class | Decreased Renal K+ Excretion [PE], Increased Diuresis [PE], Increased Diuresis [PE], Potassium-sparing Diuretic [EPC], Thiazide Diuretic [EPC], Thiazides [CS] |
| DEA Schedule | n/a |
| Marketing Category | ANDA |
| Application Number | ANDA071111 |
| Listing Certified Through | 2024-12-31 |
Package
NDC 50090-0513-00 (50090051300)
| NDC Package Code | 50090-0513-0 |
|---|---|
| Billing NDC | 50090051300 |
| Package | 28 TABLET in 1 BOTTLE (50090-0513-0) |
| Marketing Start Date | 2014-11-28 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |