Lubiprostone Capsule, Gelatin Coated
Product Images NDC 71205-831

Product Visual Gallery

This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Lubiprostone (NDC 71205-831). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Proficient Rx Lp, 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

71205-831-30 (8pdp)

Label for Lubiprostone 8 mcg capsules, gelatin coated, supplied in a package of 30 capsules. The label states each soft gel capsule contains 8 mcg of lubiprostone. Distributed by Sun Pharmaceutical Industries, Inc., Cranbury, NJ, and packaged by Proficient Rx LP, Thousand Oaks, CA. It includes handling instructions to swallow whole and storage instructions at 25°C (77°F).*

FDA Label Image

Chemical Structure (Amitiza 01)

Chemical structure diagram of lubiprostone, the active ingredient in the product Lubiprostone. The structure shows various atoms and bonds including oxygen, hydrogen, fluorine, and carbon atoms arranged in its molecular form.*

* 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.