Lubiprostone Capsule
Product Images NDC 65162-842

3 FDA label images from Amneal Pharmaceuticals Llc · 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 65162-842). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Amneal Pharmaceuticals 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

Chem Structure (Lubiprostone Capsules 1)

Chem Structure (Lubiprostone Capsules 1)
Chemical structure of lubiprostone, illustrating its molecular composition with various atoms and bonds visible.*
FDA Label Image

8 Mcg (Lubiprostone Capsules 2)

8 Mcg (Lubiprostone Capsules 2)
Lubiprostone Capsules 8 mcg oral soft gel capsule label by Amneal Pharmaceuticals LLC. The label states the active ingredient is 8 mg of lubiprostone per capsule. The label includes instructions to swallow whole and warnings to protect from extreme temperatures. It mentions the package contains 60 capsules and displays the distributor address in Bridgewater, NJ.*
FDA Label Image

24 Mcg (Lubiprostone Capsules 3)

24 Mcg (Lubiprostone Capsules 3)
Lubiprostone Capsules 24 mcg label showing dosage form as oral capsules in a 60-count package. Label includes instructions to swallow whole and not break apart or chew. Distributed by Amneal Pharmaceuticals LLC, Bridgewater, NJ. Storage instructions specify controlled room temperature from 20°C to 25°C with permitted excursions, and to protect from extreme temperatures.*

* 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.