Pantoprazole Sodium Tablet, Delayed Release
Product Images NDC 60687-736

Product Visual Gallery

This gallery contains 9 technical images submitted to the FDA as part of the official labeling for Pantoprazole Sodium (NDC 60687-736). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by American Health Packaging, 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

20 mg Pantoprazole Sodium Delayed-release Tablet Blister (20 mg Blister)

Labels for Pantoprazole Sodium delayed-release tablets, USP, 20 mg strength. Each label includes the drug name, strength, expiration and lot number placeholders, UPC barcode, and identification numbers. The labeler is American Health Packaging, Columbus, Ohio. The format repeats multiple labels on one sheet.*

FDA Label Image

20 mg Pantoprazole Sodium Delayed-release Tablets Carton (20 mg Carton)

Pantoprazole Sodium Delayed-Release Tablets, USP 20 mg in a package containing 100 tablets (10 x 10) by American Health Packaging. The label displays dosage strength, formulation type, quantity, and distributor information, including usage precautions and storage instructions.*

FDA Label Image

40 mg Pantoprazole Sodium Delayed-release Tablet Blister (40 mg Blister)

Label sheet for Pantoprazole Sodium delayed-release tablets, USP 40 mg. Each label includes the drug name, dosage strength, barcode, expiration date placeholder, lot number placeholder, and labeler information for American Health Packaging, Columbus, Ohio. The sheet contains multiple identical labels arranged in columns and rows.*

FDA Label Image

40 mg Pantoprazole Sodium Dr Tablets Carton 100 Ud (40 mg Carton 100 Ud)

Pantoprazole Sodium delayed-release tablets, USP 40 mg strength, oral tablet dosage form. The label indicates a package of 100 tablets (10 tablets per blister, 10 blisters total) with the National Drug Code (NDC) 60687-736-01. It is labeled for prescription use only and distributed by American Health Packaging, Columbus, Ohio.*

FDA Label Image

40 mg Pantoprazole Sodium Dr Tablets Carton 50 Ud (40 mg Carton 50 Ud)

Pantoprazole Sodium 40 mg delayed-release tablets, USP, oral dosage form, in a package of 50 tablets (5 x 10), labeled for prescription use only. The label includes NDC 60687-736-65 and indicates American Health Packaging as the distributor.*

FDA Label Image

40 mg Pantoprazole Sodium Dr Tablets Carton 80 Ud (40 mg Carton 80 Ud)

Label for Pantoprazole Sodium Delayed-Release Tablets, USP 40 mg, in a package of 80 tablets (8 x 10). The label includes NDC 60687-736-09 and specifies the product is Rx only. It instructs pharmacists to dispense the accompanying Medication Guide and provides storage and handling warnings. Distributed by American Health Packaging, Columbus, Ohio.*

FDA Label Image

Ahp72501

Pantoprazole Sodium 20 mg or 40 mg delayed-release oral tablets in yellow, oval-shaped form with imprint '151' on one side. The image shows both sides of the tablet but does not specify strength. Labeler is American Health Packaging.*

FDA Label Image

Ahp73601

Pantoprazole Sodium 20 mg/40 mg delayed-release oral tablets produced by American Health Packaging. The image shows two yellow, oblong tablets with one side printed with the imprint "152". A millimeter scale is included for size reference.*

FDA Label Image

Structural Formula (Structure)

Chemical structure of pantoprazole sodium, shown with a molecular diagram including functional groups and sodium ion (Na+), along with a hydration notation (1.5 H2O). The structure highlights key elements such as methoxy groups and a sulfoxide moiety.*

* 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.