Atenolol
Product Images NDC 61919-914

4 FDA label images from Direct Rx · 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 Atenolol (NDC 61919-914). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Direct Rx, 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

279 90

279 90
Label for ATENOLOL 25 mg tablets, containing 90 tablets per bottle. The label states it is generic for Tenormin and each tablet contains 25 mg atenolol USP. Packaged and distributed by Direct Rx, with storage instructions and barcode visible. Several lot numbers and expiration dates are printed on the label.*
FDA Label Image

854 90

854 90
ATENOLOL 100mg film-coated tablets packaging label for 90 tablets. The label indicates it is generic for Tenormin and each tablet contains 100mg Atenolol USP. Labeled by DIRECT RX, distributed from Dawsonville, GA. Includes lot number, discard after date, and multiple NDC codes with repeat listings of Atenolol 100mg, 90 tablets.*
FDA Label Image

914 (914 71)

914 (914 71)
The packaging label for ATENOLOL 25mg tablets, containing 100 tablets per bottle. The label states it is generic for TENORMIN and that each tablet contains 25mg of atenolol USP. The product is packaged and distributed by DIRECT RX in Alpharetta, GA.*
FDA Label Image

Image Description (Module 2)

Image Description (Module 2)
Chemical structure diagram of the active ingredient Atenolol, showing its molecular connectivity including functional groups such as hydroxyl, amine, and amide moieties attached to a benzene ring.*

* 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.