Alosetron Hydrochloride Tablet, Film Coated
Product Images NDC 73190-036

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Alosetron Hydrochloride (NDC 73190-036). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Avkare, 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 (035 30)

1 (035 30)
Alosetron Tablets USP 0.5 mg film-coated tablets package label showing 30 tablets. Label includes instructions for pharmacists, storage conditions, and manufacturer information from AvKARE. The product is for oral administration and the label features NDC 73190-035-30 with a barcode and QR code.*
FDA Label Image

2 (036 30)

2 (036 30)
Alosetron Tablets, USP 1 mg film-coated tablets in a blister pack of 30. The label indicates prescription use only and includes storage instructions to keep the product between 20° to 25°C and protect from light and moisture. The product is labeled by AvKARE and shows the NDC 73190-036-30.*
FDA Label Image

1 (Alosetron Tablets Usp 1)

1 (Alosetron Tablets Usp 1)
Chemical structure of alosetron hydrochloride, showing the arrangement of atoms and bonds within the molecule including a fused bicyclic ring system and a substituted azole ring with hydrochloride.*
FDA Label Image

1 (Alosetron Tablets Usp 2)

1 (Alosetron Tablets Usp 2)
A bar graph comparing the percent of patients between placebo and Alosetron Hydrochloride 1 mg B.I.D. in two groups of studies (Studies 1 & 2 and Studies 3 & 4). The graph shows higher patient percentages in the Alosetron group than placebo for both study groups.*

* 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.