Sumatriptan Tablet
Product Images NDC 80425-0224

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Sumatriptan (NDC 80425-0224). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Advanced Rx Of Tennessee, 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

Description (Description)

Description (Description)
Chemical structure of Sumatriptan showing its molecular composition, including indole and sulfonamide groups, along with the side chain containing dimethylamino ethyl and carboxylic acid moieties.*
FDA Label Image

Fig 1 (Figure 1)

Fig 1 (Figure 1)
A line graph showing the estimated probability of response over time in minutes from initial dose. The graph compares placebo, 25 mg, 50 mg, and 100 mg doses, with response probabilities increasing over 240 minutes for all doses except placebo, which shows a lower response.*
FDA Label Image

Fig 2 (Figure 2)

Fig 2 (Figure 2)
A line graph depicting the estimated probability of benefit or rescue over time in hours from the initial dose. It compares placebo with three dosage levels (25 mg, 50 mg, 100 mg) of a drug, showing increasing probability curves over 24 hours for each group.*
FDA Label Image

Label 1 (Sumatriptan 80425 0224 01)

Label 1 (Sumatriptan 80425 0224 01)
Sumatriptan 100 mg tablet packaging label from Advanced Rx of Tennessee, LLC. The label includes storage instructions (20-25°C), a barcode, and lot number information. It references comparison to Imitrex with corresponding NDC numbers and an expiration date of 7/31/2025. The label also shows the Aurobindo Pharma serial number.*

* 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.