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NDC 51655-0291-26 Amlodipine Besylate 5 mg/1 Details
Amlodipine Besylate 5 mg/1
Amlodipine Besylate is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Northwind Pharmaceuticals, LLC. The primary component is AMLODIPINE BESYLATE.
MedlinePlus Drug Summary
Amlodipine is used alone or in combination with other medications to treat high blood pressure in adults and children 6 years and older. It is also used to treat certain types of angina (chest pain) and coronary artery disease (narrowing of the blood vessels that supply blood to the heart). Amlodipine is in a class of medications called calcium channel blockers. It lowers blood pressure by relaxing the blood vessels so the heart does not have to pump as hard. It controls chest pain by increasing the supply of blood to the heart. If taken regularly, amlodipine controls chest pain, but it does not stop chest pain once it starts. Your doctor may prescribe a different medication to take when you have chest pain. 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: 51655-0291-26Last Updated: 04/21/2024
MedLinePlus Full Drug Details: Amlodipine
Product Information
| NDC | 51655-0291 |
|---|---|
| Product ID | 51655-291_f9894bf4-b0e8-c1e1-e053-6294a90a4b3a |
| 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 | Amlodipine Besylate |
| Proprietary Name Suffix | n/a |
| Non-Proprietary Name | Amlodipine besylate |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Dosage Form | TABLET |
| Route | ORAL |
| Active Ingredient Strength | 5 |
| Active Ingredient Units | mg/1 |
| Substance Name | AMLODIPINE BESYLATE |
| Labeler Name | Northwind Pharmaceuticals, LLC |
| Pharmaceutical Class | Calcium Channel Antagonists [MoA], Calcium Channel Blocker [EPC], Cytochrome P450 3A Inhibitors [MoA], Dihydropyridine Calcium Channel Blocker [EPC], Dihydropyridines [CS] |
| DEA Schedule | n/a |
| Marketing Category | ANDA |
| Application Number | ANDA078925 |
| Listing Certified Through | 2024-12-31 |
Package
NDC 51655-0291-26 (51655029126)
| NDC Package Code | 51655-291-26 |
|---|---|
| Billing NDC | 51655029126 |
| Package | 90 TABLET in 1 BOTTLE, PLASTIC (51655-291-26) |
| Marketing Start Date | 2023-04-03 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |