Pantoprazole Tablet, Delayed Release
Product Images NDC 55111-333

5 FDA label images from Dr.reddy's Laboratories Limited · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 5 technical images submitted to the FDA as part of the official labeling for Pantoprazole (NDC 55111-333). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Dr.reddy's Laboratories 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.

FDA Label Image

Carton1 (Carton1)

Carton1 (Carton1)
Packaging label for Pantoprazole Sodium Delayed-Release Tablets, USP 20 mg. The label indicates a package containing 30 tablets (3 blister cards of 10 tablets each) by Dr. Reddy's Laboratories Limited. The label includes storage instructions, unit-dose packaging details, and a note to dispense the medication guide to each patient.*
FDA Label Image

Carton2 (Carton2)

Carton2 (Carton2)
Packaging label of Pantoprazole Sodium delayed-release tablets USP 40 mg by Dr. Reddy's Laboratories Limited. The label shows a carton designed to contain 30 tablets (3 blister cards each with 10 tablets). Storage, dosage instructions, and handling warnings are provided. The label includes the NDC 55111-333-81 and emphasizes dispensing the medication guide with each patient.*
FDA Label Image

Container1 (Container1)

Container1 (Container1)
Pantoprazole Sodium delayed-release tablets USP 20 mg label from Dr. Reddy's Laboratories Limited. The label indicates 90 tablets per container, complete with a barcode, NDC 55111-332-90, and a QR code linking to the medication guide. Storage instructions and packaging details are also visible.*
FDA Label Image

Container2 (Container2)

Container2 (Container2)
Pantoprazole Sodium 40 mg delayed-release tablets vial label from Dr. Reddy's Laboratories Limited. The label indicates 90 tablets per container, prescription only. It includes the NDC number 55111-333-90, dosing instructions, storage conditions, and a QR code for the Medication Guide. The label is primarily white with blue and red text.*
FDA Label Image

Structure (Structure)

Structure (Structure)
Chemical structure of pantoprazole sodium sesquihydrate, the active ingredient depicted in the image, showing the molecular components including the sulfoxide group, difluoromethoxy substituent, and sodium ion with water of hydration (1.5 H2O).*

* 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.