Structure (Panto Structure)
Chemical structure of Pantoprazole Sodium shown with molecular components including sodium ion and hydration state (1.5 H2O).*
Pantoprazole Sodium
Product Images NDC 55648-434
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 55648-434). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.
As provided by Wockhardt Limited, these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.
Label (Pantoprazole Sodium Dr Tablets 20mg 100 Tablets)
Label for Pantoprazole Sodium Delayed-Release Tablets USP, 20 mg strength, in a 100-tablet package. The label includes dosage warnings, storage instructions, and manufacturer information for Wockhardt Limited. The product is marked as Rx only, with instructions to dispense with a patient information leaflet.*
Label (Pantoprazole Sodium Dr Tablets 40mg 100 Tablets)
Label for Pantoprazole Sodium Delayed-Release Tablets, USP 40 mg by WOCKHARDT LIMITED. The label shows a 100-tablet count with instructions to dispense with patient information. It includes storage information and warnings against splitting or crushing the tablets. The label features the WOCKHARDT logo and barcode.*
Label (Pantoprazole Sodium Dr Tablets 40mg 1000 Tablets)
Pantoprazole Sodium Delayed-Release Tablets, USP 40 mg, label from Wockhardt Limited. The label includes dosage and storage instructions, states the product contains 1000 tablets, and provides manufacturer and distributor details. The NDC is 64679-434-02, with a barcode and a section for lot and expiration dates.*
* 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.
