Sumatriptan Injection, Solution
Product Images NDC 83270-156

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Sumatriptan (NDC 83270-156). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Onesource Specialty 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

Carton (Carton Label)

Packaging label for Sumatriptan Injection, USP, 6 mg (base) per 0.5 mL, a subcutaneous injection solution. The label indicates single-dose vial packaging of 5 vials, produced by Onesource Specialty Pharma Limited. It includes dosage, storage instructions, and pharmacist dispensing information, emphasizing sterile, preservative-free formulation for prescription use only.*

FDA Label Image

Image Description (Image 01)

Chemical structure of sumatriptan, showing its indole-based molecular framework with a sulfonamide group and associated succinic acid moiety.*

FDA Label Image

Image-2 (Image 02)

A line graph comparing the estimated percentage of patients with relief over time in minutes between placebo and IMITREX (sumatriptan). The x-axis represents time in minutes up to 25, and the y-axis represents the estimated percentage of patients with relief from 0 to 100%. IMITREX shows a higher and more rapid increase in relief percentage compared to placebo.*

FDA Label Image

Vial (Vial Label)

Label for Sumatriptan Injection, USP, 6 mg per 0.5 mL, a subcutaneous injection solution supplied as a sterile 0.5 mL single-dose vial. Manufactured by Onesource Specialty Pharma Limited in India. The label includes prescription only status, preservative-free and nonpyrogenic indications, and directions to see package insert for usual dosage.*

* 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.