Tenormin
Product Images NDC 52427-431

4 FDA label images from Almatica Pharma Llc · 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 Tenormin (NDC 52427-431). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Almatica 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.

Product Images & Figures Index

FDA Label Image

100mg (100mg)

100mg (100mg)
Label for TENORMIN (atenolol) 100 mg tablets, containing 90 tablets. The label includes dosage instructions to take one tablet daily or as directed by a physician, storage conditions, and warnings to keep out of children's reach. The product is distributed by Almatica Pharma LLC, Morristown, NJ.*
FDA Label Image

25mg (25mg)

25mg (25mg)
TENORMIN (atenolol) 25 mg tablets label shows the product name, strength, and dosage form. The container holds 90 tablets. The label includes dosage instructions, warnings, storage conditions, and distributor information listing Almatica Pharma LLC, Morristown, NJ. It also features the NDC code 52427-429-90 and a barcode.*
FDA Label Image

50mg (50mg)

50mg (50mg)
TENORMIN (atenolol) 50 mg tablets label showing a bottle label with 90 tablets, distributed by Almatica Pharma LLC. The label includes dosage instructions, storage conditions, a barcode, and the NDC number 52427-430-90.*
FDA Label Image

Structure (Structure)

Structure (Structure)
Chemical structure of the active ingredient in TENORMIN, showing a benzene ring with attached hydroxyl, ether, amine, and amide functional groups, along with the molecular formula C14H22N2O3.*

* 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.