Pantoprazole Sodium Delayed-release Tablet
Product Images NDC 70756-019
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This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Pantoprazole Sodium Delayed-release (NDC 70756-019). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.
As provided by Lifestar Pharma 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.
40-90 (06123828 0bf3 4769 Aa39 Ba7c06b57c0f 02)
This is a product description of Pantoprazole Sodium Delayed-Release Tablets, USP. The tablets contain 40 mg of Pantoprazole and come in a bottle of 90 tablets. The medication guide must be provided separately to each patient. The tablets should not be split, chewed, or crushed. The usual dosage information is provided in the prescribing information. The tablets should be stored at 20° to 25°C (68° to 77°F) and kept in a tight, light-resistant container that is child-resistant. The manufacturer is Lifestar Pharma LLC, located in Mahwah, NJ, and the product is made in India. For the medication guide, visit www.lifestarpharma.com/medguide/pantoprazolesodiumtablets.pdf or scan the QR code.*
40-1000 (06123828 0bf3 4769 Aa39 Ba7c06b57c0f 03)
This is a description of a medication named Pantoprazole Sodium. It is a delayed-release tablet and should be swallowed whole. The Pharmacist should dispense the medication guide separately for each patient. The usual dosage should be consulted as per the accompanying prescribing information. It is to be stored at a temperature of 20° to 25°C (68° to 77°F) and should be kept away from children. It is manufactured for Lifestar Pharma LLC and made in India. There is also a code No given.*
* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.