Mycophenolic Acid Tablet, Delayed Release
Product Images NDC 82293-013

View Photos of 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 Mycophenolic Acid (NDC 82293-013). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Novugen Pharma (usa) 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.

FDA Label Image

Bottle Label (Image01)

Bottle Label (Image01)
Mycophenolic Acid Delayed-Release Tablets, USP 180 mg, bottle label by Novugen Pharma (USA) LLC. The label states each delayed-release tablet contains mycophenolate sodium USP equivalent to 180 mg mycophenolic acid. The label specifies storage instructions, child-resistant packaging, and includes NDC code 82293-012-10 with a quantity of 120 tablets. The product is distributed by Novugen Pharma in NJ and made in India.*
FDA Label Image

Bottle Label (Image02)

Bottle Label (Image02)
Mycophenolic Acid Delayed-Release Tablets, USP 360 mg, in a tablet bottle label. The label shows the product name, strength, dosage form, and a count of 120 tablets. It includes storage instructions, distributor information (Novugen Pharma USA LLC), and a barcode. The label states the product is Rx only and made in India.*
FDA Label Image

Image Description (Structure 01)

Image Description (Structure 01)
Chemical structure of Mycophenolic Acid displayed as a molecular diagram showing atoms and bonds, including hydroxyl, methoxy, methyl, and sodium carboxylate functional groups.*

* 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.