Theophylline Tablet, Extended Release
Product Images NDC 60219-2045

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 60219-2045). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Amneal Pharmaceuticals Ny 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.

Product Images & Figures Index

FDA Label Image

Hb (Theophylline Extended Release Tablets 300 mg And 4 1)

Hb (Theophylline Extended Release Tablets 300 mg And 4 1)
Chemical structure of theophylline, showing its molecular framework with nitrogen and oxygen atoms arranged in the characteristic xanthine ring system.*
FDA Label Image

1 (Theophylline Extended Release Tablets 300 mg And 4 2)

1 (Theophylline Extended Release Tablets 300 mg And 4 2)
Theophylline Extended-Release Tablets 300 mg oral dosage form in a package of 100 tablets. The label indicates these are uncoated, extended-release tablets. The product is manufactured by Amneal Pharmaceuticals Pvt. Ltd. and distributed by Amneal Pharmaceuticals LLC. Storage and child-resistant packaging instructions are included on the label.*
FDA Label Image

1 (Theophylline Extended Release Tablets 300 mg And 4 3)

1 (Theophylline Extended Release Tablets 300 mg And 4 3)
Label for Theophylline Extended-Release Tablets 450 mg, supplied by Amneal Pharmaceuticals NY LLC. The label indicates 100 tablets, extended-release, oral route, with child-resistant packaging. It includes storage instructions and manufacturer details, showing a beige and white design with the Amneal logo.*

* 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.