Sulfamethoxazole And Trimethoprim Injection, Solution, Concentrate
Product Images NDC 70069-361

Product Visual Gallery

This gallery contains 8 technical images submitted to the FDA as part of the official labeling for Sulfamethoxazole And Trimethoprim (NDC 70069-361). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Somerset Therapeutics, Llc, 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

Molecular Structure (trimethoprim)

Chemical structure diagram of the active ingredients sulfamethoxazole and trimethoprim, showing the molecular arrangement of atoms and bonds in these compounds.*

FDA Label Image

Molecular Structure (sulfamethoxazole)

Chemical structure diagram showing the molecular components of Sulfamethoxazole and Trimethoprim, the active ingredients in this prescription drug injection solution concentrate by Somerset Therapeutics, LLC.*

FDA Label Image

5 mL Container Label (012dfac7 9b72 48a5 A364 E62bbe150cfe 03)

Label for Sulfamethoxazole and Trimethoprim Injection, USP, showing strengths of 400 mg/5 mL sulfamethoxazole and 80 mg/5 mL trimethoprim. This is a 5 mL single-dose vial for intravenous infusion only. Manufactured for Somerset Therapeutics, LLC, made in India. The label includes storage instructions and dilution requirements before administration.*

FDA Label Image

Carton Label (10 X 5 mL Single-dose Vials) (012dfac7 9b72 48a5 A364 E62bbe150cfe 04)

Packaging label for Sulfamethoxazole and Trimethoprim Injection, USP, an intravenous solution by Somerset Therapeutics, LLC. The label indicates strengths of 400 mg/5 mL for sulfamethoxazole and 80 mg/5 mL for trimethoprim in single-dose vials, with a package containing ten 5 mL vials. Storage and formulation details, including preservatives and instructions to dilute with 5% dextrose injection, are also visible.*

FDA Label Image

10 mL Container Label (012dfac7 9b72 48a5 A364 E62bbe150cfe 05)

Label for Sulfamethoxazole and Trimethoprim Injection, USP, containing 800 mg/10 mL sulfamethoxazole and 160 mg/10 mL trimethoprim in a 10 mL multiple-dose vial for intravenous infusion. Manufactured for Somerset Therapeutics, LLC. Includes storage and usage instructions, barcode, and regulatory information.*

FDA Label Image

Carton Label (10 X 10 mL Single-dose Vials) (012dfac7 9b72 48a5 A364 E62bbe150cfe 06)

Label for Sulfamethoxazole and Trimethoprim Injection, USP, 800 mg/10 mL sulfamethoxazole and 160 mg/10 mL trimethoprim (80 mg/mL and 16 mg/mL), injection solution concentrate for intravenous use. Pack contains 10 multiple-dose vials of 10 mL each. Manufactured for Somerset Therapeutics, LLC. Includes storage instructions, ingredient details, and usage precautions.*

FDA Label Image

30 mL Container Label (012dfac7 9b72 48a5 A364 E62bbe150cfe 07)

Label for Sulfamethoxazole and Trimethoprim Injection, USP, an intravenous solution concentrate. Contains 2,400 mg/30 mL sulfamethoxazole (80 mg/mL) and 480 mg/30 mL trimethoprim (16 mg/mL). Supplied in a 30 mL multiple-dose vial. Manufactured for Somerset Therapeutics, LLC, Somerset, NJ. Directions note dilution with 5% dextrose prior to administration and storage at 20° to 25°C.*

FDA Label Image

Carton Label (30 mL Multiple-dose Vial) (012dfac7 9b72 48a5 A364 E62bbe150cfe 08)

Packaging label for Sulfamethoxazole and Trimethoprim Injection, USP, a 30 mL multiple-dose vial injection solution. Contains sulfamethoxazole 2400 mg/30 mL (80 mg/mL) and trimethoprim 480 mg/30 mL (16 mg/mL). For intravenous infusion only, must be diluted with 5% dextrose injection before administration. Manufactured for Somerset Therapeutics LLC, with storage instructions and preservative content details included on the label.*

* 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.