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Pantoprazole Sodium Tablet, Delayed Release
Product Images NDC 64980-677
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Product Visual Gallery
This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Pantoprazole Sodium (NDC 64980-677). 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.
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This is a description of Pantoprazole Sodium Delayed-Release Tablets, USP (20 mg) containing 90 tablets. The tablets should be swallowed whole and not split, chewed, or crushed. They should be stored at a temperature range of 20° to 25°C (68° to 77°F), with excursions permitted to 15° to 30°C (59° to 86°F). The medication guide can be obtained from the manufacturer's website. The tablets are manufactured by Graviti Pharmaceuticals Pvt. Ltd. in India and distributed by Rising Pharma Holdings, Inc. in East Brunswick.*
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This text provides specific information about a medication called Pantoprazole, which is typically prescribed to treat various gastrointestinal conditions. It includes details on the dosage, formulation type (coated tablets), dosage instructions, storage conditions, manufacturer details, and distribution information. Additionally, it emphasizes the importance of not splitting, chewing, or crushing the tablets and highlights the proper way to consume them. The text also mentions the availability of a Medication Guide for this medication, which is recommended for dispensing to patients. It is advisable to follow the given dosage instructions and storage recommendations mentioned in the text for effective and safe use of the medication.*
* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.
