Atenolol Tablet
Product Images NDC 0378-0218

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Atenolol (NDC 0378-0218). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Mylan Pharmaceuticals 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

Atenolol Tablets, Usp 25 mg Bottle Label (Image 01)

Chemical structure of atenolol, the active ingredient in Atenolol tablets. The diagram shows the molecular arrangement including aromatic and amide groups.*

FDA Label Image

Atenolol Tablets, Usp 50 mg Bottle Label (Image 02)

Atenolol Tablets USP 25 mg oral tablets label from Mylan Pharmaceuticals Inc. The label shows one 25 mg tablet marked 'A2', with a package count of 100 tablets. It includes storage instructions and dispensing information, emphasizing child-resistant packaging and controlled room temperature storage. The NDC number 0378-0218-01 is displayed.*

FDA Label Image

Atenolol Tablets, Usp 100 mg Bottle Label (Image 03)

Atenolol 50 mg oral tablets label by Mylan Pharmaceuticals Inc. The label indicates the product name Atenolol Tablets, USP, with strength of 50 mg. It contains 100 tablets and is prescription-only. The label includes the NDC code 0378-0231-01 and safety storage instructions. A small round white tablet with imprint "231" is pictured.*

FDA Label Image

Image 04

Atenolol 100 mg oral tablets label from Mylan Pharmaceuticals Inc., containing 100 tablets. The label includes the NDC number 0378-0757-01 and states the tablets are USP standard. Instructions mention dispensing in a light-resistant container and storage conditions. The label also features a barcode and dosage information.*

* 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.