Tenormin Tablet
Product Images NDC 24979-246

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Tenormin (NDC 24979-246). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Upsher-smith Laboratories, 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

Structure (Structure)

Chemical structure diagram of Atenolol with molecular formula C14H22N2O3, showing the arrangement of atoms including a benzene ring, hydroxyl group, and amide substituents.*

FDA Label Image

100mg (Tenormin 100mg)

TENORMIN (Atenolol) 100 mg tablets label features the strength prominently on a green background and states it contains 90 tablets. The label includes the NDC number, manufacturer (Norwich Pharmaceuticals, Inc.), distributor (TWi Pharmaceuticals USA, Inc.), storage instructions, and warnings about keeping the medication out of reach of children. The label also notes the usual dosage and prescription status (Rx only).*

FDA Label Image

25mg (Tenormin 25mg)

TENORMIN (atenolol) 25 mg tablets label for oral use, containing 90 tablets. The label includes dosage instructions, storage conditions, and manufacturer details. The product is labeled as Rx only and distributed by TWi Pharmaceuticals USA, Inc.*

FDA Label Image

50mg (Tenormin 50mg)

TENORMIN (atenolol) 50 mg tablets label displays a package containing 90 tablets. It includes dosage instructions, a warning to keep out of reach of children, and storage conditions at 20° to 25°C. The label shows the manufacturer as Norwich Pharmaceuticals, Inc., and distributor as TWi Pharmaceuticals USA, Inc.*

* 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.