Pantoprazole Sodium Tablet, Delayed Release
Product Images NDC 80425-0278

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Pantoprazole Sodium (NDC 80425-0278). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Advanced Rx Pharmacy Of Tennessee, 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.

FDA Label Image

Description (Description)

Description (Description)
Chemical structure diagram of pantoprazole sodium showing the molecular components including fluorinated benzene ring, sulfone group, pyridine ring, and associated sodium ion and water of hydration (1.5 H2O).*
FDA Label Image

Label 2 (Pantoprazole Sodium Dr 80425 0278 02)

Label 2 (Pantoprazole Sodium Dr 80425 0278 02)
Pantoprazole Sodium 20 mg delayed-release tablets package label. Displays product name, strength, dosage form, quantity (#60), and comparison to Protonix. Includes NDC numbers, lot, and expiration date. Labeler is Advanced Rx Pharmacy of Tennessee, LLC, located in Nashville, TN.*
FDA Label Image

Label 3 (Pantoprazole Sodium Dr 80425 0278 03)

Label 3 (Pantoprazole Sodium Dr 80425 0278 03)
Pantoprazole Sodium DR 20 mg delayed release tablets packaging label showing the Advanced Rx Pharmacy of Tennessee, LLC as labeler. The label indicates a quantity of 90 tablets, with storage instructions to keep between 20–25°C. It includes a barcode, lot number 90PAN20724, and expiration date 7/31/2024. The label notes this product is comparable to Protonix and provides associated NDC codes.*
FDA Label Image

* 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.