Lubiprostone Capsule, Gelatin Coated
Product Images NDC 76420-907

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Lubiprostone (NDC 76420-907). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Asclemed Usa, 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.

Product Images & Figures Index

FDA Label Image

Chemical Structure (Amitiza 01)

Chemical Structure (Amitiza 01)
Chemical structure of lubiprostone, the active ingredient in the drug Lubiprostone. The diagram shows the molecular arrangement, including oxygen, hydrogen, fluorine atoms, and carbon chains.*
FDA Label Image

Label (Lubiprostone 24mcg)

Label (Lubiprostone 24mcg)
Labels for Lubiprostone Capsules 24 mcg by Enovachem Pharmaceuticals are shown in multiple package sizes including 30, 60, 90, and 100 count. The capsules are gelatin-coated, orange, and the labels include the NDC numbers and instructions to store at controlled room temperature. Sun Pharmaceutical Industries, Inc. is listed as the distributor.*
FDA Label Image

Label (Lubiprostone 8mcg)

Label (Lubiprostone 8mcg)
This image shows multiple packaging labels for Lubiprostone Capsules 8 mcg by Enovachem Pharmaceuticals. The gelatin-coated capsules are available in quantities of 30, 60, 90, and 100 per package. Labels display the NDC numbers, distributor as Sun Pharmaceutical Industries, Inc., and emphasize prescription status with storage instructions at controlled room temperature.*

* 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.