Atenolol
Product Images NDC 13107-170

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Atenolol (NDC 13107-170). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Aurolife Pharma 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

Package Label-principal Display Panel (25 mg (1000 Tablet Bottle))

Atenolol Tablets USP 25 mg label manufactured by Aurolife Pharma LLC and Aurobindo Pharma USA, Inc. The label states each tablet contains 25 mg Atenolol USP, includes usual dosage instructions, warnings, storage conditions, and batch and expiry fields. The package contains 1000 tablets. The label also features barcode and the Aurobindo logo.*

FDA Label Image

Package Label-principal Display Panel (50 mg (1000 Tablet Bottle))

Atenolol Tablets, USP 50 mg label showing a package of 1000 tablets. The label includes storage instructions, dosage directions stating one tablet daily or as directed, and a warning to keep out of reach of children. Manufactured by Aurolife Pharma LLC and for Aurobindo Pharma USA, Inc., Dayton, NJ. The label features the Aurobindo logo and an NDC code 13107-169-99.*

FDA Label Image

Package Label-principal Display Panel (100 mg (1000 Tablet Bottle))

Label for Atenolol Tablets USP 100 mg, containing 1000 tablets. Manufactured by Aurolife Pharma LLC and Aurobindo Pharma USA, Inc., Dayton, NJ. Includes dosage instructions, warnings, storage conditions, and batch/expiry placeholder text. Features barcodes and Aurobindo logo.*

FDA Label Image

Chemical Structure (Atenolol Str)

Chemical structure of Atenolol showing its molecular formula C14H22N2O3 with functional groups and ring structures.*

* 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.