Sumatriptan
Product Images NDC 50090-1605

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 Sumatriptan (NDC 50090-1605). 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 (Lbl500901605)

Label Image (Lbl500901605)
Sumatriptan Injection 6 mg per 0.5 mL single-dose vials packaged in a box from A-S Medication Solutions. The label indicates six 0.5 mL single-dose vials containing sumatriptan succinate equivalent to 6 mg sumatriptan. Storage instructions specify refrigeration at 36°F to 46°F. Product NDC is 50090-1605.*
FDA Label Image

Figure 1. Time To Relief Of Cluster Headache From Time Of Injectiona (Sumatriptan Fig1)

Figure 1. Time To Relief Of Cluster Headache From Time Of Injectiona (Sumatriptan Fig1)
A line graph comparing the estimated percentage of subjects with relief over time between placebo and Sumatriptan Injection groups. The x-axis represents time in minutes (0 to 25), and the y-axis shows the percentage of subjects with relief from 0% to 100%. Two lines depict the data: one for placebo and one for Sumatriptan Injection, indicating increasing relief percentage over time for both, with Sumatriptan Injection showing greater relief throughout.*
FDA Label Image

Sumatriptan Chemical Structure (Sumatriptan Str)

Sumatriptan Chemical Structure (Sumatriptan Str)
Chemical structure of sumatriptan showing its molecular framework, including an indole ring, sulfonamide group, and side chains as represented in the image.*

* 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.