Eletriptan Hydrobromide
Product Images NDC 55700-756

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Eletriptan Hydrobromide (NDC 55700-756). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Quality Care Products, 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

1

Label for Eletriptan Hydrobromide Tablets 40 mg, distributed by Quality Care Products, LLC. The package contains 6 unit dose tablets. The label includes storage instructions to keep at 68 to 77 degrees F and states the product is Rx only. Marketed by Ajanta Pharma USA Inc., Bridgewater, NJ.*

FDA Label Image

Fig_1 (Eletriptan Fig1)

A line graph titled 'Estimated Probability of Initial Headache Response Within 2 Hours' showing the estimated probability of response on the y-axis over time in hours from the initial dose on the x-axis. The graph compares response probabilities for double blind placebo and eletriptan hydrobromide at doses of 20 mg, 40 mg, and 80 mg, with higher doses showing increased probability of response over two hours.*

FDA Label Image

Fig_2 (Eletriptan Fig2)

A line graph showing the estimated probability of taking a second dose or other medication over 24 hours from the initial dose. The x-axis represents time in hours, and the y-axis represents probability. The graph compares data for double blind placebo, eletriptan 20 mg, eletriptan 40 mg, and eletriptan 80 mg doses.*

FDA Label Image

Str (Eletriptan Str)

Chemical structure of eletriptan hydrobromide, showing the molecular components including an indole ring, sulfonamide group, and hydrobromide salt.*

* 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.