Pantoprazole Sodium Tablet, Delayed Release
Product Images NDC 85509-1636

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This gallery contains 2 technical images submitted to the FDA as part of the official labeling for Pantoprazole Sodium (NDC 85509-1636). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Phoenix Rx 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.

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FDA Label Image

Label (16336)

Label (16336)
This is a detailed description of Pantoprazole Sodium Delayed-Release Tablets. Each tablet contains 20 mg of pantoprazole. The recommended dosage information can be found by scanning the QR code on the package insert. It is essential to swallow the tablets whole and not to split, chew, or crush them. The storage temperature is between 20°C to 25°C with excursions permitted to 15°C to 30°C. The tablets must be stored at USP Controlled Room Temperature. Pharmacists should dispense a Medication Guide to each patient. The tablets come in a package of 60 tablets and are prescription-only. The manufacturer is Amneal Pharmaceuticals Pvt. Ltd., repackaged by PHOENIX RX LLC in Hatboro, PA, USA. The NDC number is 85509-1636-6. The tablets' expiration date indicated is July 10, 2026.*
FDA Label Image

1 (Pantoprazole Sodium Delayed Release Tablets Usp 1)

1 (Pantoprazole Sodium Delayed Release Tablets Usp 1)

* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.