Alosetron Tablet
Product Images NDC 70756-702

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Alosetron (NDC 70756-702). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Lifestar Pharma 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

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Chemical structure of Alosetron hydrochloride, depicting the molecular arrangement including a fused bicyclic system and an imidazole ring with associated functional groups, based on the provided product data.*

FDA Label Image

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A bar graph comparing the percent of patients for placebo versus Alosetron 1 mg tablets taken twice daily (B.I.D) across two groups of clinical studies. The graph shows higher percentages for patients on Alosetron in Studies 1 & 2 and Studies 3 & 4 compared to placebo.*

FDA Label Image

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Label for Alosetron Tablets, USP 0.5 mg, oral tablet by Lifestar Pharma LLC. The label states each film-coated tablet contains 0.5 mg Alosetron Hydrochloride equivalent, with a package count of 30 tablets. Storage instructions specify 20° to 25°C (68° to 77°F) and protection from light and moisture. It includes a medication guide notice and barcode.*

FDA Label Image

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Alosetron Tablets, USP 1 mg oral tablets package label by Lifestar Pharma LLC, containing 30 tablets. The label includes storage instructions (20° to 25°C), a dosage note referencing prescribing information, and caution about dispensing with a Medication Guide. Manufactured for Lifestar Pharma LLC, Mahwah, NJ, made in India. Includes barcode and QR code for 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.