Lubiprostone Capsule, Gelatin Coated
Product Images NDC 80425-0355

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Lubiprostone (NDC 80425-0355). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Advanced Rx Of Tennessee, 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

Label 1 (Lubiprostone 24mcg 80425 0355 02)

Label 1 (Lubiprostone 24mcg 80425 0355 02)
Lubiprostone 24 mcg capsule gelatin coated, labeled for oral use. The packaging compares this product to AMITIZA and provides NDC numbers 80425-0355-02 and source NDC 63304-0352-60. It includes lot and expiration date information, specifying an expiration of 8/16/2023. The labeler is Advanced Rx of Tennessee, LLC, based in Nashville, TN. The package count is 60 capsules.*
FDA Label Image

Chemical Structure (Amitiza 01)

Chemical Structure (Amitiza 01)
Chemical structure diagram of the active ingredient lubiprostone, showing its molecular framework including oxygen, fluorine, and hydrogen atoms arranged in a specific pattern.*

* 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.