Lubiprostone Capsule, Gelatin Coated
Product Images NDC 43598-168

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 43598-168). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Dr. Reddy's Laboratories 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.

FDA Label Image

Chemical Structure (Lubiprostone 01)

Chemical Structure (Lubiprostone 01)
Chemical structure of the active ingredient Lubiprostone. The diagram shows the molecular arrangement including functional groups such as ketones, hydroxyl groups, and fluorinated alkyl side chains.*
FDA Label Image

Principal Display Panel (8 mcg Capsule Bottle Label)

Principal Display Panel (8 mcg Capsule Bottle Label)
Lubiprostone 8 mcg Capsules carton with 60 capsules. The label shows the product name, strength, quantity, and distribution by Dr. Reddy's Laboratories Inc., Princeton, NJ. Instructions include swallowing whole without breaking or chewing and storage precautions. The label includes an NDC barcode and states the capsules are gelatin coated for oral use.*
FDA Label Image

Principal Display Panel (24 mcg Capsule Bottle Label)

Principal Display Panel (24 mcg Capsule Bottle Label)
Label for Lubiprostone Capsules 24 mcg by Dr. Reddy's Laboratories Inc. The label indicates a package of 60 oral gelatin-coated capsules, each containing 24 mcg of lubiprostone. It includes storage instructions, cautions against breaking or chewing capsules, and notes the active ingredient is made in Japan and encapsulated in the US.*

* 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.