Esomeprazole Magnesium Capsule, Delayed Release
Product Images NDC 16571-880

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 Esomeprazole Magnesium (NDC 16571-880). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Rising Pharma Holdings, 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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ESOMEPRAZOLE MAGNESIUM delayed-release capsules, 20 mg, manufactured by Graviti Pharmaceuticals Pvt. Ltd., India, and distributed by Rising Pharma Holdings, Inc. The label states the product is an acid reducer that treats frequent heartburn and contains 14 capsules, representing a one 14-day course of treatment. It includes warnings, directions for use, and contact information for questions.*
FDA Label Image

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Packaging label for Esomeprazole Magnesium Delayed-Release Capsules USP, 20 mg, by Rising Pharma Holdings, Inc. The product is an oral capsule available in a bottle containing 14 capsules for a one 14-day course of treatment. The label highlights it as an acid reducer that treats frequent heartburn, with dosage and safety information included.*
FDA Label Image

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Packaging label for Esomeprazole Magnesium delayed-release capsules USP 20 mg by Rising Pharma Holdings, Inc. The label features the brand name Rising and indicates the product is an acid reducer to treat frequent heartburn. It contains 42 capsules, intended for a three 14-day course of treatment, with directions to take 1 to 4 capsules daily for full effect. The label also includes Drug Facts and warnings, barcode, and NDC 16571-880-42.*

* 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.