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NDC 51655-0695-52 valsartan 160 mg/1 Details

valsartan 160 mg/1

valsartan is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Northwind Pharmaceuticals. 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: 51655-0695-52
Last Updated: 04/21/2024
MedLinePlus Full Drug Details: Valsartan

Product Information

NDC	51655-0695
Product ID	51655-695_db47e55b-d403-ac9e-e053-2a95a90a94c0
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	valsartan
Proprietary Name Suffix	n/a
Non-Proprietary Name	valsartan
Product Type	HUMAN PRESCRIPTION DRUG
Dosage Form	TABLET
Route	ORAL
Active Ingredient Strength	160
Active Ingredient Units	mg/1
Substance Name	VALSARTAN
Labeler Name	Northwind Pharmaceuticals
Pharmaceutical Class	Angiotensin 2 Receptor Antagonists [MoA], Angiotensin 2 Receptor Blocker [EPC]
DEA Schedule	n/a
Marketing Category	ANDA
Application Number	ANDA203536
Listing Certified Through	2024-12-31

Package

NDC 51655-0695-52 (51655069552)

Pricing Information	N/A
NDC Package Code	51655-695-52
Billing NDC	51655069552
Package	30 TABLET in 1 BOTTLE, PLASTIC (51655-695-52)
Marketing Start Date	2021-03-23
NDC Exclude Flag	N