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NDC 51655-0310-53 Furosemide 20 mg/1 Details
Furosemide 20 mg/1
Furosemide is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Northwind Pharmaceuticals, LLC. 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: 51655-0310-53Last Updated: 04/21/2024
MedLinePlus Full Drug Details: Furosemide
Product Information
| NDC | 51655-0310 |
|---|---|
| Product ID | 51655-310_f2b92056-ca3e-c5c6-e053-2995a90a9973 |
| Associated GPIs | |
| 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 | 20 |
| Active Ingredient Units | mg/1 |
| Substance Name | FUROSEMIDE |
| Labeler Name | Northwind Pharmaceuticals, LLC |
| Pharmaceutical Class | Increased Diuresis at Loop of Henle [PE], Loop Diuretic [EPC] |
| DEA Schedule | n/a |
| Marketing Category | ANDA |
| Application Number | ANDA076796 |
| Listing Certified Through | 2024-12-31 |
Package
NDC 51655-0310-53 (51655031053)
| NDC Package Code | 51655-310-53 |
|---|---|
| Billing NDC | 51655031053 |
| Package | 10 TABLET in 1 BOTTLE, PLASTIC (51655-310-53) |
| Marketing Start Date | 2022-11-28 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |