Theophylline Tablet, Extended Release
Product Images NDC 31722-077

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Theophylline (NDC 31722-077). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Camber 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
FDA Label Image

Theophylline300mglabel (Theophylline300mglabel)

Theophylline300mglabel (Theophylline300mglabel)
Theophylline Extended-Release Tablets 300 mg label from Camber Pharmaceuticals, Inc. The label indicates an uncoated extended-release oral tablet, packaged as 100 tablets in a container with a child-resistant closure. It includes storage instructions and a U.S. contact number, along with manufacturer details. The NDC is 31722-077-01.*
FDA Label Image

Theophylline450mglabel (Theophylline450mglabel)

Theophylline450mglabel (Theophylline450mglabel)
Theophylline Extended-Release Tablets 450 mg label from Camber Pharmaceuticals, Inc. Indicates 100 tablets per container for oral use. Includes details like dosage form, strength, NDC 31722-078-01, and storage instructions. Features a barcode and contact information along with manufacturer details in Piscataway, NJ, and By: Annora Pharma Pvt. Ltd. in India.*
FDA Label Image

Theophyllineertabletsstructure (Theophyllineertabletsstructure)

Theophyllineertabletsstructure (Theophyllineertabletsstructure)
Chemical structure diagram of the active ingredient Theophylline, depicting its molecular arrangement with carbon, nitrogen, oxygen atoms, and methyl 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.