Pantoprazole Sodium Tablet, Delayed Release
Product Images NDC 65862-560

5 FDA label images from Aurobindo Pharma 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 Sodium (NDC 65862-560). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Aurobindo Pharma 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

Package Label-principal Display Panel (20 mg (90 Tablets Bottle))

Package Label-principal Display Panel (20 mg (90 Tablets Bottle))
Label for Pantoprazole Sodium Delayed-Release Tablets, USP 20 mg by Aurobindo Pharma Limited. The label specifies the dose strength as 20 mg, for prescription use only, with 90 tablets per container. It includes storage instructions, pharmacist dispensing information, and distributor details for Aurobindo Pharma USA, Inc. The label also has a barcode and notes about printing and coding areas.*
FDA Label Image

Package Label-principal Display Panel (20 mg Blister Carton (10 x 10 Unit-dose))

Package Label-principal Display Panel (20 mg Blister Carton (10 x 10 Unit-dose))
Pantoprazole Sodium Delayed-Release Tablets, USP 20 mg carton label for unit-dose tablets. The label indicates 100 tablets packaged as (10 x 10) unit-dose tablets. The labeler is Aurobindo Pharma Limited, with distribution by Aurobindo Pharma USA, Inc. It includes the Rx only designation and a barcode on the side panel.*
FDA Label Image

Package Label-principal Display Panel (40 mg (90 Tablets Bottle))

Package Label-principal Display Panel (40 mg (90 Tablets Bottle))
Label for Pantoprazole Sodium Delayed-Release Tablets USP 40 mg by Aurobindo Pharma Limited. The label includes dosage information, storage instructions, and distributor details for Aurobindo Pharma USA, Inc. It specifies that tablets should not be split, chewed, or crushed, and to store at controlled room temperature. The label also indicates 90 tablets in the container.*
FDA Label Image

Package Label-principal Display Panel (40 mg Blister Carton (10 x 10 Unit-dose))

Package Label-principal Display Panel (40 mg Blister Carton (10 x 10 Unit-dose))
Packaging label for Pantoprazole Sodium Delayed-Release Tablets, USP 40 mg by Aurobindo Pharma Limited. The label indicates this is a unit-dose tablet package containing 100 tablets (10 x 10). The label prominently features the strength '40 mg' and instructions indicating prescription-only status with a note for pharmacists to dispense the medication guide separately.*
FDA Label Image

Chemical Structure (Pantoprazole Str)

Chemical Structure (Pantoprazole Str)
Chemical structure of Pantoprazole Sodium, showing its molecular configuration including aromatic rings, a sulfoxide group, and sodium ion, with associated 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.