Pantoprazole Tablet, Delayed Release
Product Images NDC 67296-2355

6 FDA label images from Redpharm Drug · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 6 technical images submitted to the FDA as part of the official labeling for Pantoprazole (NDC 67296-2355). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Redpharm Drug, 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

Structure (Structure)

Structure (Structure)
Chemical structure of pantoprazole sodium sesquihydrate, showing its molecular components including sulfoxide and substituted pyridine and benzimidazole rings.*
FDA Label Image

Container1 (Container1)

Container1 (Container1)
Pantoprazole Sodium delayed-release tablets, USP 20 mg in a blister pack label containing 90 tablets. The label includes NDC 55111-332-90, directions for pharmacists to dispense the medication guide, storage instructions, and manufacturing information by Dr. Reddy's Laboratories Limited, India. The label features a QR code and barcode.*
FDA Label Image

Carton1 (Carton1)

Carton1 (Carton1)
Packaging label for Pantoprazole Sodium Delayed-Release Tablets, USP 20 mg by Dr. Reddy's. The box contains 30 tablets (3 blisters of 10 unit-dose tablets). The label includes dosing instructions, storage conditions, pharmacist dispensing advisory, and manufacturing details from Dr. Reddy's Laboratories Limited, India.*
FDA Label Image

Container2 (Container2)

Container2 (Container2)
Pantoprazole Sodium Delayed-Release Tablets, USP 40 mg carton label showing dosage strength prominently in red, with a package count of 90 tablets. Includes dispensing instruction for pharmacists to provide the Medication Guide to each patient. The label includes storage instructions, a QR code for the Medication Guide, barcode, and is labeled for Dr. Reddy's Laboratories Limited with an FDA NDC code 555111-333-90.*
FDA Label Image

1000scontainer (1000scontainer)

1000scontainer (1000scontainer)
Pantoprazole Sodium Delayed-Release Tablets, USP 40 mg tablet label for oral use by Redpharm Drug, shown in a tablet bottle label format. Contains 1000 tablets with pharmacist medication guide instructions and storage details, including temperature and handling warnings. Features text, barcode, QR code for Medication Guide, and manufacturer information from Dr. Reddy's Laboratories Limited.*
FDA Label Image

Carton2 (Carton2)

Carton2 (Carton2)
The packaging label for Pantoprazole Sodium Delayed-Release Tablets, USP 40 mg, manufactured by Dr. Reddy's Laboratories Limited. The label includes product name, dosage strength, tablet count (30 tablets in 3 blister cards), pharmacist dispensing instructions, storage conditions, and barcode. The label is primarily white with blue and red text and includes the Dr. Reddy's logo.*

* 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.