Theophylline Tablet, Extended Release
Product Images NDC 46708-026

3 FDA label images from Alembic Pharmaceuticals Limited · 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 46708-026). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Alembic Pharmaceuticals Limited, 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

300 mg 30" Hdpe Bottle (Theophylline 300mg)

300 mg 30" Hdpe Bottle (Theophylline 300mg)
Theophylline Extended-Release Tablets, 300 mg strength, in a package containing 30 tablets. Manufactured by Alembic Pharmaceuticals Limited. The label includes storage instructions, dosage form as uncoated extended-release tablets, and states the product is for prescription use only. NDC number 46708-025-30 is visible.*
FDA Label Image

450 mg 30" Hdpe Bottle (Theophylline 450mg)

450 mg 30" Hdpe Bottle (Theophylline 450mg)
Theophylline Extended-Release Tablets 450 mg in a package of 30 tablets. The label indicates the active ingredient as Theophylline (Anhydrous) USP 450 mg per tablet. Manufactured by Alembic Pharmaceuticals Limited, India, this oral extended-release formulation comes with storage instructions and a child-resistant container closure. The label includes the NDC 46708-026-30 and Alembic logo.*
FDA Label Image

Structure (Theophylline Str)

Structure (Theophylline Str)
Chemical structure diagram of the active ingredient Theophylline, showing its molecular composition and arrangement, consistent with the known xanthine derivative form.*

* 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.