Sulfamethoxazole And Trimethoprim Tablet
Product Images NDC 50090-2201

3 FDA label images from A-s Medication Solutions · 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 Sulfamethoxazole And Trimethoprim (NDC 50090-2201). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by A-s Medication Solutions, 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

Label Image (Lbl500902201)

Label Image (Lbl500902201)
The packaging label for Sulfamethoxazole and Trimethoprim UTI-PAK tablets shows a double strength of 800 mg/160 mg. The label includes details such as the quantity of 6 tablets, the product NDC code 50090-2201-0, and the manufacturer A-S Medication Solutions LLC in Libertyville, IL. It also features warnings, storage instructions at 68-77 degrees F, and a barcode.*
FDA Label Image

Sulfamethoxazole Chemical Structure (Sulfatrime Str1)

Sulfamethoxazole Chemical Structure (Sulfatrime Str1)
Chemical structure of Sulfamethoxazole, an active ingredient in Sulfamethoxazole and Trimethoprim tablets. The diagram shows the molecular arrangement including an amino group, sulfonamide group, and an isoxazole ring with a methyl substituent.*
FDA Label Image

Trimethoprim Chemical Structure (Sulfatrime Str2)

Trimethoprim Chemical Structure (Sulfatrime Str2)
Chemical structure diagram of Sulfamethoxazole and Trimethoprim, depicting the molecular arrangement of the active ingredients shown in the product data.*

* 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.