Valsartan Tablet, Film Coated
Product Images NDC 65862-571

Product Visual Gallery

This gallery contains 9 technical images submitted to the FDA as part of the official labeling for Valsartan (NDC 65862-571). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Aurobindo Pharma Limited, these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.

FDA Label Image

Valsartan Fig1 (Valsartan Fig1)

A forest plot chart illustrating effects on mortality amongst subgroups in the VALIANT study. The chart compares Valsartan versus Captopril across various subgroups, including age, gender, ethnicity, geographic location, and beta-blocker use, with a central vertical line at 1.0 indicating no difference between treatments.*

FDA Label Image

Package Label-principal Display Panel (40 mg (30 Tablet Bottle))

Label for Valsartan Tablets USP 40 mg film-coated tablets, packaged in a bottle of 30 tablets. The label includes storage instructions, distributor information (Aurobindo Pharma USA, Inc.), and notes that the product is made in India by Aurobindo Pharma Limited. It also indicates prescription-only status and contains a barcode on the right side.*

FDA Label Image

Package Label-principal Display Panel (40 mg Blister Carton (10 x 10 Unit-dose))

Packaging label for Valsartan Tablets USP 40 mg film-coated tablets. The label specifies a quantity of 100 (10 x 10) unit-dose tablets. The labeler is Aurobindo Pharma Limited. The label includes the NDC 65862-570-10 and states the product is Rx only.*

FDA Label Image

Package Label-principal Display Panel (80 mg (90 Tablet Bottle))

Label for Valsartan Tablets USP 80 mg film-coated tablets by Aurobindo Pharma Limited, containing 90 tablets. The label states the product is prescription only, provides storage instructions (20° to 25°C), and advises dispensing in a tight container. Distributed by Aurobindo Pharma USA, Inc.*

FDA Label Image

Package Label-principal Display Panel (80 mg Blister Carton (10 x 10 Unit-dose))

Packaging carton for Valsartan Tablets USP 80 mg film-coated tablets. The label shows a unit-dose tablet count of 100 (10 x 10). The labeler is Aurobindo Pharma Limited, with distribution noted by Aurobindo Pharma USA, Inc. The carton includes dosage form, strength, and manufacturer information.*

FDA Label Image

Package Label-principal Display Panel (160 mg (90 Tablet Bottle))

Label for Valsartan Tablets USP 160 mg film-coated tablets by Aurobindo Pharma Limited. The label states 90 tablets per container, includes storage instructions, and is marked Rx only. Distributed by Aurobindo Pharma USA, Inc., made in India, with an NDC 65862-572-90 barcode present.*

FDA Label Image

Valsartan-fig7 (Valsartan Fig7)

Packaging label for Valsartan Tablets USP 160 mg film-coated tablets by Aurobindo Pharma Limited. The carton indicates a quantity of 100 unit-dose tablets (10 x 10) with the strength prominently displayed in an orange oval. The label includes the NDC 65862-572-10 and states the product is Rx only.*

FDA Label Image

Package Label-principal Display Panel (320 mg (90 Tablet Bottle))

Label for Valsartan Tablets USP 320 mg film-coated tablets by Aurobindo Pharma Limited. The label indicates 90 tablets per container, includes storage instructions (20° to 25°C), and distribution information for Aurobindo Pharma USA, Inc. The NDC number 65862-573-90 is displayed along with a note to refer to the package insert for dosage.*

FDA Label Image

Chemical Structure (Valsartan Str)

Chemical structure of Valsartan, showing its molecular configuration with characteristic phenyl and tetrazole rings attached to the side chains, consistent with the active ingredient in the product label.*

* About these descriptions: Image descriptions on this page are generated by automated AI analysis of the product label images from the manufacturer's FDA label submission (SPL). They are provided for reference only and may contain errors or omissions. Always rely on the printed label itself and the official FDA labeling, and consult a pharmacist or healthcare professional with any questions about this product.