Mesalamine Capsule, Extended Release
Product Images NDC 67877-717

3 FDA label images from Ascend Laboratories, Llc · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Mesalamine (NDC 67877-717). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Ascend Laboratories, Llc, these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.

Product Images & Figures Index

FDA Label Image

Mesalamine 120cap

Mesalamine 120cap
Mesalamine Extended-Release Capsules, USP 0.375 g label from Ascend Laboratories, LLC. The label indicates each capsule contains 0.375 g mesalamine, is for oral extended-release use, and the package contains 120 capsules. Storage instructions and manufacturer information from Alkem Laboratories Ltd., India, are provided along with the product NDC 67877-717.*
FDA Label Image

Mesalamine 500cap

Mesalamine 500cap
Label for Mesalamine Extended-Release Capsules, USP 0.375 g by Ascend Laboratories, LLC. Each capsule contains 0.375 g of mesalamine in an extended-release oral capsule form. The label states Rx only, packaging quantity of 500 capsules, storage instructions, manufacturer Alkem Laboratories Ltd. India, and distributor Ascend Laboratories, Parsippany, NJ. The label includes an NDC number 67877-717-05 and a barcode.*
FDA Label Image

Mesalamine Structure

Mesalamine Structure
Chemical structure showing the molecular formula of mesalamine, featuring an aromatic benzene ring with an amino group, hydroxyl groups, and a carboxylic acid functional group. This corresponds to the active ingredient mesalamine.*

* 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.