Theophylline
Product Images NDC 71321-502

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Theophylline (NDC 71321-502). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Brandywine 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

Label 100 mg (T 100 mg)

Theophylline Extended-Release Tablets label showing 100 mg strength. The label indicates the package contains 100 tablets and is distributed by Brandywine Pharmaceuticals, LLC. The label includes storage instructions, dosage reference, a barcode, and a warning to keep out of reach of children.*

FDA Label Image

Label 200 mg (T 200 mg)

Theophylline Extended-Release Tablets 200 mg label from Brandywine Pharmaceuticals, LLC. The label indicates a package of 100 tablets, Rx only, containing 200 mg of Theophylline (Anhydrous) USP per tablet. Storage instructions specify 20° to 25°C (68° to 77°F). The label includes warnings and instructions for dispensing in child-resistant containers.*

FDA Label Image

Label 300 mg (T 300)

Theophylline Extended-Release Tablets 300 mg label from Brandywine Pharmaceuticals, LLC. The label states the product contains 300 mg of theophylline, is prescription only, and includes 100 tablets per container. It provides storage instructions, a warning to keep out of reach of children, and the manufacturer's location in West Chester, PA. The NDC number and barcode are visible.*

FDA Label Image

Theophylline (Theophylline Structure)

Chemical structure of Theophylline, showing a xanthine derivative with methyl and keto groups in its molecular framework.*

* 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.