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NDC 51660-0141-03 VALSARTAN 80 mg/1 Details
VALSARTAN 80 mg/1
VALSARTAN is a ORAL TABLET, FILM COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Ohm Laboratories Inc.. The primary component is VALSARTAN.
MedlinePlus Drug Summary
Valsartan is used in adults and in children 1 year of age and older alone or in combination with other medications to treat high blood pressure. It is also used in adults to treat heart failure (condition in which the heart is unable to pump enough blood to the rest of the body) and to improve survival after a heart attack. Valsartan is in a class of medications called angiotensin II receptor antagonists. It works by blocking the action of certain natural substances that tighten the blood vessels, allowing the blood to flow more smoothly and the heart to pump more efficiently. 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: 51660-0141-03Last Updated: 11/30/2022
MedLinePlus Full Drug Details: Valsartan
Product Information
| NDC | 51660-0141 |
|---|---|
| Product ID | 51660-141_0ea6cbb4-10cd-fecf-e063-6394a90a513b |
| Associated GPIs | 36150080000320 |
| GCN Sequence Number | 048401 |
| GCN Sequence Number Description | valsartan TABLET 80 MG ORAL |
| HIC3 | A4F |
| HIC3 Description | ANTIHYPERTENSIVES, ANGIOTENSIN RECEPTOR ANTAGONIST |
| GCN | 13846 |
| HICL Sequence Number | 012204 |
| HICL Sequence Number Description | VALSARTAN |
| Brand/Generic | Generic |
| Proprietary Name | VALSARTAN |
| Proprietary Name Suffix | n/a |
| Non-Proprietary Name | VALSARTAN |
| Product Type | HUMAN PRESCRIPTION DRUG |
| Dosage Form | TABLET, FILM COATED |
| Route | ORAL |
| Active Ingredient Strength | 80 |
| Active Ingredient Units | mg/1 |
| Substance Name | VALSARTAN |
| Labeler Name | Ohm Laboratories Inc. |
| Pharmaceutical Class | Angiotensin 2 Receptor Antagonists [MoA], Angiotensin 2 Receptor Blocker [EPC] |
| DEA Schedule | n/a |
| Marketing Category | ANDA |
| Application Number | ANDA077492 |
| Listing Certified Through | 2025-12-31 |
Package
NDC 51660-0141-03 (51660014103)
| NDC Package Code | 51660-141-03 |
|---|---|
| Billing NDC | 51660014103 |
| Package | 10 TABLET, FILM COATED in 1 BOTTLE (51660-141-03) |
| Marketing Start Date | 2014-07-07 |
| NDC Exclude Flag | N |
| Pricing Information | N/A |