Theophylline
Product Images NDC 29033-001

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 29033-001). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Nostrum Laboratories, 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

Theophylline Structural Formula (Image 01)

Theophylline Structural Formula (Image 01)
Chemical structure of Theophylline (Anhydrous) showing the molecular arrangement of carbon, nitrogen, oxygen, and hydrogen atoms with labeled atom positions.*
FDA Label Image

Theophylline (anhydrous) Extended-release Tablets 400 mg Bottle Label (Image 02)

Theophylline (anhydrous) Extended-release Tablets 400 mg Bottle Label (Image 02)
Theophylline (Anhydrous) Extended-Release Tablets label showing 400 mg strength. The label indicates each tablet contains 400 mg of Theophylline, USP, with a package count of 100 tablets. The product is manufactured by Nostrum Laboratories, Inc., Kansas City, MO. The label includes storage instructions, a prescription only statement, and a barcode.*
FDA Label Image

Theophylline (anhydrous) Extended-release Tablets 600 mg Bottle Label (Image 03)

Theophylline (anhydrous) Extended-release Tablets 600 mg Bottle Label (Image 03)
Label for Theophylline (Anhydrous) Extended-Release Tablets containing 600 mg per tablet. The label states the product is manufactured by Nostrum Laboratories, Inc. and contains 100 tablets per container. It includes storage instructions, a warning to keep out of reach of children, and specifies that it is for prescription use only (Rx Only).*

* 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.