Sulfamethoxazole And Trimethoprim Tablet
Product Images NDC 65862-420

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Sulfamethoxazole And Trimethoprim (NDC 65862-420). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Aurobindo Pharma 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.

FDA Label Image

Package Label-principal Display Panel (400 mg/80 mg (100 Tablet Bottle))

Label for Sulfamethoxazole and Trimethoprim Tablets, USP, 400 mg/80 mg, supplied as 100 tablets by Aurobindo Pharma Limited. The label shows tablet strengths, storage instructions, and distribution details for Aurobindo Pharma USA, Inc., including storage temperature and packaging requirements.*

FDA Label Image

Package Label-principal Display Panel (800 mg/160 mg (100 Tablet Bottle))

Label for Sulfamethoxazole and Trimethoprim Tablets, USP, 800 mg/160 mg double strength, 100 tablets. Distributed by Aurobindo Pharma USA, Inc., made in India. Storage instructions and dispensing guidelines are also visible along with the NDC 65862-420-01.*

FDA Label Image

Sulfamethoxazole Chemical Structure (Sulfatrime Str1)

Chemical structure diagram of the active ingredient sulfamethoxazole and trimethoprim. The structure displays molecular bonds and groups typical to these compounds used in drug formulations by Aurobindo Pharma Limited.*

FDA Label Image

Trimethoprim Chemical Structure (Sulfatrime Str2)

Chemical structure diagram of sulfamethoxazole and trimethoprim, showing the molecular arrangement of atoms and bonds for these active ingredients used in tablets by Aurobindo Pharma Limited.*

* 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.