Theophylline Tablet, Extended Release
Product Images NDC 82804-941

3 FDA label images from Proficient Rx Lp · 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 82804-941). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Proficient Rx Lp, 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

82804-941-30 (Image 01)

82804-941-30 (Image 01)
Theophylline 400 mg extended-release tablets label by Proficient Rx LP. The label states each tablet contains 400 mg of Theophylline (Anhydrous), USP, with 30 tablets per package. Tablets are described as white, round, bisected, debossed with 'N' above and 'T4' below the bisect. Manufactured by MPP Pharma, LLC, Kansas City, MO, with storage instructions at 20°-25°C (68°-77°F).*
FDA Label Image

82804-942-30 (Image 02)

82804-942-30 (Image 02)
Theophylline 600 mg extended-release tablets label from Proficient Rx. The label indicates a count of 30 tablets per container. Tablets are described as white, oblong, bisected on one side and debossed with "NT6" on the other. Manufactured by MPP Pharma LLC in Kansas City, MO. Storage instructions specify 20°-25°C (68°-77°F). The label includes barcodes and a statement to keep medication out of reach of children.*
FDA Label Image

Chemical Structure (Theophylline 01)

Chemical Structure (Theophylline 01)
Chemical structure of the active ingredient theophylline anhydrous, showing its molecular framework with numbered atoms and functional groups including methyl and carbonyl groups.*

* 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.