Valsartan Tablet, Film Coated
Product Images NDC 71335-2151

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 5 technical images submitted to the FDA as part of the official labeling for Valsartan (NDC 71335-2151). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Bryant Ranch Prepack, 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

Camberlogo1 (Camberlogo1)

FDA Label Image

Camberlogo2 (Camberlogo2)

FDA Label Image

Label (Lbl713352151)

Label (Lbl713352151)
Label for Valsartan 40 mg tablet, film-coated, packaged by Bryant Ranch Prepack in Burbank, CA. The label references comparison to Diovan 40 mg tablet from Hetero Labs Limited, includes storage instructions to keep at room temperature (20°-25°C), and advises keeping drugs out of reach of children. The package count is 30 tablets, with the NDC 71335-2151 visible on the label along with a barcode.*
FDA Label Image

Valsartantabfig1 (Valsartantabfig1)

Valsartantabfig1 (Valsartantabfig1)
A forest plot graph comparing Valsartan versus Captopril outcomes across various patient subgroups including age, gender, ethnicity, and treatment with beta-blockers. The x-axis ranges from 0.5 (favoring Valsartan) to 1.5 (favoring Captopril) with a central line at 1.0 representing no difference. Each subgroup shows a point estimate with confidence intervals.*
FDA Label Image

Valsartantabstructure (Valsartantabstructure)

Valsartantabstructure (Valsartantabstructure)
Chemical structure of the active ingredient Valsartan, showing a detailed molecular formula diagram with various aromatic rings and functional groups.*

* 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.