Theophylline Tablet, Extended Release
Product Images NDC 69367-415

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Theophylline (NDC 69367-415). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Westminster Pharmaceuticals, 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

Chemical Structure (Theophylline 01)

Chemical Structure (Theophylline 01)
Chemical structure of the active ingredient theophylline anhydrous, showing its molecular arrangement with nitrogen, oxygen, carbon, and hydrogen atoms depicted in a bicyclic structure.*
FDA Label Image

Principal Display Panel (400 mg Tablet Bottle Label)

Principal Display Panel (400 mg Tablet Bottle Label)
Label for Theophylline (Anhydrous) Extended-Release Tablets, 400 mg strength, manufactured by Westminster Pharmaceuticals, LLC. The label indicates a package size of 100 tablets and includes storage instructions and a warning to keep out of reach of children. The label displays the NDC number 69367-414-01 and the product is marked Rx Only.*
FDA Label Image

Principal Display Panel (600 mg Tablet Bottle Label)

Principal Display Panel (600 mg Tablet Bottle Label)
Theophylline (Anhydrous) Extended-Release Tablets 600 mg in tablet extended release form, packaged as 100 tablets. The label includes storage instructions, dosage reference, and a warning to keep medication out of reach of children. Manufactured by Westminster Pharmaceuticals, LLC, the label displays the NDC 69367-415-01 and features a barcode.*

* 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.