Diovan
Product Images NDC 67544-403

Product Visual Gallery

This gallery contains 5 technical images submitted to the FDA as part of the official labeling for Diovan (NDC 67544-403). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Aphena Pharma Solutions - Tennessee, Llc, 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

Bottle Label 80mg (67544 403)

Label for Diovan (Valsartan) 80 mg tablets, containing 30 tablets. The label includes storage instructions, manufacturer information noting Novartis Pharmaceuticals Corp., East Hanover, NJ, and repackager Aphena Pharma Solutions - Tennessee, LLC, Cookeville, TN 38506. It also indicates the product is Rx only and includes multiple barcodes and the NDC number 67544-0403-30.*

FDA Label Image

Bottle Label 160mg (67544 404)

Label for Diovan, containing 160 mg of Valsartan in tablet form. The package includes 30 tablets. Manufactured by Novartis Pharmaceuticals Corp., repackaged by Aphena Pharma Solutions - Tennessee, LLC. The label provides storage instructions and states the product is for prescription use only.*

FDA Label Image

Aphena Pharma Solutions (TN)

FDA Label Image

Valsartan Structural Formula (Diovan Tablets 01)

Chemical structure of valsartan, the active ingredient in Diovan.*

FDA Label Image

Effects On Mortality Amongst Subgroups In Valiant (Diovan Tablets 02)

A forest plot comparing Valsartan versus Captopril outcomes across various patient subgroups including age, gender, race, geography, and beta-blocker use. The plot displays point estimates with confidence intervals indicating relative favorability for each treatment.*

* 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.