Mycophenolic Acid Tablet, Delayed Release
Product Images NDC 16729-261

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Mycophenolic Acid (NDC 16729-261). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Accord Healthcare 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

Package Label – 180 mg (Mycophenolic Acid 180mg 120)

Mycophenolic Acid 180 mg delayed release tablets label by Accord Healthcare Inc. The label includes dosage form, strength, and storage instructions. It states the product contains Mycophenolate Sodium USP equivalent to Mycophenolic Acid 180 mg per film-coated tablet, with 120 tablets per package. It includes warnings to store at controlled room temperature, protect from moisture, and dispense in a tight container. The label shows NDC 16729-261-29 and manufacturer information including Intas Pharmaceuticals Limited, India.*

FDA Label Image

Package Label – 360 mg (Mycophenolic Acid 360mg 120)

Mycophenolic Acid Delayed Release Tablets, USP 360 mg oral tablets label by Accord Healthcare Inc. The label includes storage instructions at 20°C to 25°C, dosage guidance to see package insert, warning to keep out of reach of children, and manufacturer information for Intas Pharmaceuticals Limited in India. The package contains 120 tablets and has space allocated for lot and expiration data, plus barcodes.*

FDA Label Image

Chemical Structure (Mycophenolic Acid Structure)

Chemical structure of Mycophenolic Acid sodium salt, depicting the molecular arrangement relevant to the active ingredient in the medication Mycophenolic Acid.*

* 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.