Sulfamethoxazole And Trimethoprim Suspension
Product Images NDC 17856-0496

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Sulfamethoxazole And Trimethoprim (NDC 17856-0496). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Atlantic Biologicals Corp., 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

17856 0496 02

Label for Sulfamethoxazole and Trimethoprim Oral Suspension, USP 400 mg/80 mg per 10 mL, from Atlantic Biologicals Corp. The label shows storage instructions to keep between 20° to 25°C (68° to 77°F) and protect from light. The dosage listed is 10 mL, with a quantity of 72 cups. It includes barcode, GTIN, serial number, expiration date (06/05/21), lot number, and contact information for reorder.*

FDA Label Image

17856 0496 03

Label for Sulfamethoxazole and Trimethoprim oral suspension USP, with a strength of 800 mg/160 mg per 20 mL. The label includes storage instructions to keep at controlled room temperature (20° to 25°C) and protect from light. The product is packaged in 50 cups, distributed by Atlantic Biologicals Corp., Miami, FL, and includes a barcode and unit dose serialization details.*

FDA Label Image

Stru1 (Sulfatrime Str1)

Chemical structure of Sulfamethoxazole as part of the Sulfamethoxazole and Trimethoprim active ingredients shown in the image.*

FDA Label Image

Stru2 (Sulfatrime Str2)

Chemical structure of Sulfamethoxazole and Trimethoprim, the active ingredients of this product. The diagram shows the molecular structures with atoms and bonds as typically represented in chemical formula illustrations.*

* 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.