Imitrex Tablet, Film Coated
Product Images NDC 0173-0736

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 6 technical images submitted to the FDA as part of the official labeling for Imitrex (NDC 0173-0736). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Glaxosmithkline 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

Imitrex Tablets Chemical Structure (Imitrex Spl Graphic 01)

FDA Label Image

Figure 1 (Imitrex Spl Graphic 02)

FDA Label Image

Figure 2 (Imitrex Spl Graphic 03)

FDA Label Image

Imitex 25mg 9 Count Carton (Imitrex Spl Graphic 04)

Imitex 25mg 9 Count Carton (Imitrex Spl Graphic 04)
This is a product description for tablets containing 25 mg of sumatriptan, with NDC number 0173-0735-00 for identification. The brand name of the product is not available. There are 9 tablets per container.*
FDA Label Image

Imitex 50mg 9 Count Carton (Imitrex Spl Graphic 05)

Imitex 50mg 9 Count Carton (Imitrex Spl Graphic 05)
This is a packaging information of Ronly containing 9 tablets. Each tablet contains 70 mg of sumatriptan succinate equivalent to 50 mg of sumatriptan. The National Drug Code (NDC) for this product is 0173-0736-01.*
FDA Label Image

Imitex 100mg 9 Count Carton (Imitrex Spl Graphic 06)

Imitex 100mg 9 Count Carton (Imitrex Spl Graphic 06)
This is a medication with the National Drug Code (NDC) 0173-0737-01, known as "Ronly sawieanmamamion TABLETS". Each tablet contains 4 succinate equivalent to 100 mg of sumatriptan, and the package includes 9 tablets.*

* 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.