Sumatriptan Injection
Product Images NDC 70594-068

View Photos of 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 Sumatriptan (NDC 70594-068). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Xellia Pharmaceuticals Usa 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

Chemical Structure (Sumatriptan 01)

Chemical Structure (Sumatriptan 01)
Chemical structure of sumatriptan succinate, showing the molecular arrangement including indole ring and sulfonamide group, with succinate acid moiety indicated.*
FDA Label Image

Figure 1 (Sumatriptan 02)

Figure 1 (Sumatriptan 02)
Line graph depicting the estimated percentage of patients with relief over time (0 to 25 minutes) comparing Sumatriptan injection and placebo. The graph shows time in minutes on the x-axis and percentage of patients on the y-axis, with Sumatriptan represented by circles and placebo by squares.*
FDA Label Image

Principal Display Panel (6 mg/0.5 mL Vial Carton)

Principal Display Panel (6 mg/0.5 mL Vial Carton)
Packaging label for Sumatriptan Injection USP 6 mg/0.5 mL, a subcutaneous injection. The label indicates it is a prescription drug supplied as 5 single-dose vials of 0.5 mL each. It is manufactured for Xellia Pharmaceuticals USA LLC and notes the product is made in India. The label includes directions to discard unused portions and store between 2° to 30°C, with additional caution to protect from light and retain in carton until use.*

* 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.