Alosetron Hydrochloride Tablet
Product Images NDC 71930-010

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Alosetron Hydrochloride (NDC 71930-010). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Eywa Pharma Inc, 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

05mg (05mg)

Alosetron Tablets, USP 0.5 mg film-coated oral tablets in a 30-count package by Eywa Pharma Inc. The label shows dosage strength, NDC 71930-010-30, dispensing instructions, storage conditions, and distributor and manufacturer information. Marked for pharmacist dispensing with accompanying Medication Guide.*

FDA Label Image

1mg (1mg)

Label for Alosetron Hydrochloride Tablets, USP 1 mg oral tablets, containing 30 film-coated tablets. The label includes NDC 71930-011-30, storage instructions at 20° to 25°C, and cautions to keep medication out of reach of children. Distributed by Eywa-Hibrow Pharma, manufactured by WES Pharma Inc.*

FDA Label Image

Alo-str.jpg (Aloset Struc)

Chemical structure of Alosetron Hydrochloride depicting its molecular framework with rings, methyl groups, and a hydrochloride component, consistent with the active ingredient in the drug product.*

FDA Label Image

Fig1 (Alosetron Tablets Figure 1)

A bar chart comparing the percent of patients for placebo and Alosetron Tablets 1 mg taken twice daily (B.I.D.) across two study groupings: Studies 1 & 2 and Studies 3 & 4. The chart shows higher patient percentages for Alosetron in both study sets.*

* 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.