Telmisartan Tablet
Product Images NDC 71335-1723

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 6 technical images submitted to the FDA as part of the official labeling for Telmisartan (NDC 71335-1723). 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

Image-1 (Image 1)

Image-1 (Image 1)
Packaging label image showing Telmisartan tablets, USP, 20 mg strength. The image depicts hand-held blister cards with printed barcodes, expiration dates, and lot numbers. The product is oral dosage form tablets, distributed by Bryant Ranch Prepack, with visible labeling details for individual tablets in blister packaging.*
FDA Label Image

Image-2 (Image 2)

Image-2 (Image 2)
An instructional illustration showing hands peeling open a protective foil or blister pack to access a single tablet inside, demonstrating the method to remove the tablet from its packaging by pressing down and lifting the foil.*
FDA Label Image

Label (Lbl713351723)

Label (Lbl713351723)
Label for Telmisartan 80 mg tablet by Bryant Ranch Prepack in Burbank, CA. The label indicates it is a generic equivalent to Micardis 80 mg tablets by Glenmark Pharmaceuticals. It includes lot number 1523487, storage instructions at 20°-25°C, a barcode, and a quantity of 90 tablets. The product is for Rx use only.*
FDA Label Image
FDA Label Image

Logo1

FDA Label Image

Structure (Structure)

Structure (Structure)
Chemical structure of Telmisartan shown as a molecular diagram with rings and functional groups, including carboxyl and methyl groups, consistent with its known molecular framework.*

* 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.