Alosetron Hydrochloride Tablet, Film Coated
Product Images NDC 65162-248

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Alosetron Hydrochloride (NDC 65162-248). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Amneal Pharmaceuticals 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

Alosetron Tablets Usp 1

Chemical structure of Alosetron Hydrochloride depicted as a 2D molecular diagram showing its atomic connectivity and functional groups.*

FDA Label Image

Alosetron Tablets Usp 2

A bar chart depicting the percent of patients in placebo versus Alosetron Hydrochloride 1 mg B.I.D. groups across two study sets. Studies 1 & 2 show 19% for placebo and 32% for Alosetron. Studies 3 & 4 show 29% for placebo and 50% for Alosetron.*

FDA Label Image

Alosetron Tablets Usp 3

Packaging label for Alosetron Tablets, USP 0.5 mg film-coated tablets by Amneal Pharmaceuticals LLC. The label states the dosage strength as 0.5 mg, includes a visual of an oval tablet imprinted with 'AN248', and indicates a package size of 30 tablets. Storage instructions specify 20° to 25°C (68° to 77°F) with protection from light and moisture. The label also notes distribution by Amneal Pharmaceuticals in Bridgewater, NJ.*

FDA Label Image

Alosetron Tablets Usp 4

Alosetron Hydrochloride 1 mg film-coated tablets label showing a blue, oval tablet imprinted with AN249. The label states the strength as 1 mg per tablet and indicates a package size of 30 tablets. The product is distributed by Amneal Pharmaceuticals LLC and includes storage instructions and a note to dispense with an attached medication guide.*

* 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.