Telmisartan Tablet
Product Images NDC 70518-2572

4 FDA label images from Remedyrepack Inc. · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Telmisartan (NDC 70518-2572). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Remedyrepack Inc., 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

Remedy_label (Remedy Label)

Remedy_label (Remedy Label)
Telmisartan 80 mg tablet label showing a quantity of 30 moisture sensitive tablets. The label includes warnings about not removing tablets from blisters until immediately before administration. It is labeled for prescription use only and repackaged by RemedyRepack Inc. Additional packaging information includes source manufacturer Glenmark in Mahwah, NJ.*
FDA Label Image

Image-1 (Image 1)

Image-1 (Image 1)
Packaging label of Telmisartan Tablet USP, 20 mg strength, in a blister pack. The image shows individual tablets labeled with the product name, strength, and barcodes on each blister cavity. The labeler is RemedyRepack Inc.*
FDA Label Image

Image-2 (Image 2)

Image-2 (Image 2)
An instructional line drawing showing a hand pressing down on a tablet package to push a tablet out of its blister pack. A downward arrow indicates the motion needed to release the tablet from the packaging.*
FDA Label Image

Structure (Structure)

Structure (Structure)
Chemical structure of telmisartan, showing its molecular framework with several aromatic rings and functional groups including a carboxylic acid, methyl groups, and nitrogen-containing heterocycles.*

* 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.