Atenolol
Product Images NDC 61919-279

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 61919-279). 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

279-30 (279 30)

279-30 (279 30)
Packaging label for ATENOLOL 25 mg tablets, containing 30 tablets. The label indicates it is a generic for TENORMIN, with each tablet containing 25 mg atenolol USP. Distributed by DirectRx, with sample lot and expiration details shown. The label warns that the medication is prescription-only and to keep out of reach of children.*
FDA Label Image

72189 0146 30

72189 0146 30
ATENOLOL 25mg tablet bottle label with a count of 30 tablets. The label states ATENOLOL as the proprietary name, notes it is generic for TENORMIN, and specifies each tablet contains 25mg Atenolol USP. The packaging is distributed by DirectRx and includes lot and expiration date details, as well as manufacturing and NDC codes.*
FDA Label Image

72189 0146 60

72189 0146 60
ATENOLOL 25 mg 60 tablets label indicates it is generic for Tenormin. Each tablet contains atenolol 25 mg USP. The label shows lot number, expiration date 11/30/22, packaging and distribution by DirectRx, and manufacturing details from Mylan Pharmaceuticals Inc., Dawsonville, GA. The packaging also includes NDC 72189-146-60 and cautions about federal law prohibiting transfer and storage instructions.*
FDA Label Image

72189 0146 90

72189 0146 90
Label for Atenolol 25 mg tablets, 90 count, generic for Tenormin. Label shows dosage strength, quantity, and directions to store between 68-77 degrees Fahrenheit. Packaged and distributed by DirectRx, with lot number 29SE2008 and expiration date 11/30/22. Includes FDA cautionary statements and manufacturing details.*

* 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.