Pentasa Capsule
Product Images NDC 54092-189

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Pentasa (NDC 54092-189). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Takeda Pharmaceuticals America, Inc., 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

Pentasa 01

Chemical structure of mesalamine, the active ingredient in Pentasa 250 mg and 500 mg oral capsules by Takeda Pharmaceuticals America, Inc. The structure shows a benzene ring with amino, hydroxyl, and carboxyl functional groups attached.*

FDA Label Image

Principal Display Panel (250 mg Capsule Bottle Label)

Pentasa 250 mg extended-release capsules packaging label showing 240 capsules. The product contains the active ingredient mesalamine and is labeled for prescription use only. It is distributed by Takeda Pharmaceuticals America, Inc. The label includes dosage information, warnings, and storage instructions.*

FDA Label Image

Principal Display Panel (500 mg Capsule Bottle Label)

Label for Pentasa (mesalamine) extended-release capsules, 500 mg strength, manufactured by Takeda Pharmaceuticals America, Inc. The label indicates a package containing 120 capsules with prescription-only status. The design features a blue and white color scheme with the Takeda logo and includes dosing and storage information.*

FDA Label Image

Principal Display Panel (500 mg Capsule Sample Carton)

Packaging label for Pentasa (mesalamine) 500 mg controlled-release capsules by Shire US Inc. The box contains 8 capsules and is marked as a patient sample, not for sale. The label includes storage instructions, patient instructions space, a barcode, and manufacturer information.*

* 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.