Lansoprazole Tablet, Orally Disintegrating
Product Images NDC 68382-771

Product Visual Gallery

This gallery contains 5 technical images submitted to the FDA as part of the official labeling for Lansoprazole (NDC 68382-771). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Zydus Pharmaceuticals 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.

FDA Label Image

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FDA Label Image

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FDA Label Image

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This is a visual representation of the mean severity of night heartburn over the course of three days from the start of treatment with either a 15mg or 30mg dose of Lansoprazole, a medication used to treat GERD and other acid-related conditions. The chart shows improvement in heartburn severity with either dose of the medication.*

FDA Label Image

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This is a package insert for Lansoprazole Orally Disintegrating Tablets. Each tablet contains 15mg Lansoprazole in delayed-release form. The tablets should not be chewed, but placed on the tongue until they disintegrate and can be swallowed. The medication guide is available at the manufacturer's website. The tablets are not child-resistant and should be kept out of the reach of children. There are patient instructions on how to take the tablets, and an alternative method of delivery is through a syringe. The package contains 100 tablets.*

FDA Label Image

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This is a package of Lansoprazole delayed-release orally disintegrating tablets. The tablets should not be chewed. They can be swallowed whole or allowed to dissolve slowly in the mouth. The package contains 100 tablets divided into 10x10 unit-dose packages. Additional patient instructions are not available due to poor quality.*

* 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.