Theophylline
Product Images NDC 10135-604

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Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Theophylline (NDC 10135-604). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Marlex Pharmaceuticals 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 Is Structurally Classified As A Methylxanthine. It Occurs As A White, Odorless, Crystalline Powder With A Bitter Taste. Anhydrous Theophylline Has The Chemical Name 1h-purine- 2,6-dione, 3,7-dihydro-1 ,3 –dimethyl-, And Is Represented By The Following Structural Formula: (Theophylline 01)

Theophylline Is Structurally Classified As A Methylxanthine. It Occurs As A White, Odorless, Crystalline Powder With A Bitter Taste. Anhydrous Theophylline Has The Chemical Name 1h-purine- 2,6-dione, 3,7-dihydro-1 ,3 –dimethyl-, And Is Represented By The Following Structural Formula: (Theophylline 01)
Chemical structure of theophylline, showing its molecular framework with nitrogen atoms and ketone groups in a fused bicyclic ring system.*
FDA Label Image

Principal Display Panelndc 10135-0604-08theophyllineoral Solution, Usp80 mg/ 15 mL (Theophylline 02)

Principal Display Panelndc 10135-0604-08theophyllineoral Solution, Usp80 mg/ 15 mL (Theophylline 02)
Label for Theophylline Oral Solution, USP by Marlex Pharmaceuticals Inc. The label states each 15 mL contains 80 mg theophylline anhydrous. The solution is alcohol-free and comes in a 473 mL (16 ounces) bottle. The label includes storage instructions, dosage notes to individualize use, and child-resistance warnings. The NDC number 10135-0604-08 is shown.*

* 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.