Mycophenolate Mofetil Capsule
Product Images NDC 64380-726

3 FDA label images from Strides Pharma Science Limited · 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 Mycophenolate Mofetil (NDC 64380-726). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Strides Pharma Science Limited, 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

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2887b6a8 C8f2 4a4e A789 92418486569a 01
Chemical structure of mycophenolate mofetil shown as a 2D molecular diagram with labeled atoms and bonds, illustrating its chemical composition and arrangement.*
FDA Label Image

2887b6a8 C8f2 4a4e A789 92418486569a 02

2887b6a8 C8f2 4a4e A789 92418486569a 02
Label for Mycophenolate Mofetil Capsules, USP 250 mg by Strides Pharma Science Ltd. The label specifies a package of 100 oral capsules, includes storage instructions at 20°-25°C, a caution on handling and disposal, and a note to pharmacists to dispense the medication guide. It features manufacturer and distributor information from India and the USA, with a barcode and space for batch details.*
FDA Label Image

2887b6a8 C8f2 4a4e A789 92418486569a 03

2887b6a8 C8f2 4a4e A789 92418486569a 03
Label for Mycophenolate Mofetil Tablets USP, 500 mg, oral capsules by Strides Pharma Science Limited. The label indicates a package size of 100 tablets, includes storage instructions (20°-25°C), usage caution, and directions to dispense the accompanying medication guide. Manufactured in Bengaluru, India, and distributed by Strides Pharma Inc., East Brunswick, NJ.*

* 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.