Alosetron Hydrochloride Tablet, Film Coated
Product Images NDC 53746-249

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Alosetron Hydrochloride (NDC 53746-249). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Amneal Pharmaceuticals Of New York 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 (Alosetron Tablets Usp 1)

Chemical structure of Alosetron Hydrochloride showing its molecular arrangement including nitrogen-containing rings and the HCl salt form representation.*

FDA Label Image

1 (Alosetron Tablets Usp 2)

A bar graph comparing the percent of patients in placebo versus Alosetron Hydrochloride 1 mg B.I.D. groups across two sets of studies labeled 'Studies 1 & 2' and 'Studies 3 & 4.' The vertical axis shows percent of patients from 0 to 100, with higher response percentages for Alosetron Hydrochloride in both study sets.*

FDA Label Image

1 (Alosetron Tablets Usp 3)

Alosetron Tablets, USP 0.5 mg film-coated tablets, oral dosage form, packaged as 30 tablets. The label includes dosing, storage instructions (store at 20° to 25°C), and a medication guide link. Manufactured by Amneal Pharmaceuticals of New York LLC, the label also features the Amneal logo and NDC 53746-248-30.*

FDA Label Image

1 (Alosetron Tablets Usp 4)

Alosetron Tablets, USP 1 mg film-coated tablets in a rectangular carton. The label shows an image of a blue, oval tablet imprinted with 'AH 249'. It states the product is prescription only, contains 30 tablets per bottle, and is manufactured by Amneal Pharmaceuticals of New York LLC. Storage instructions specify 20° to 25°C and protection from light and moisture.*

* 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.