Diclofenac Sodium And Misoprostol Tablet, Film Coated
Product Images NDC 59762-0028

4 FDA label images from Mylan Pharmaceuticals Inc. · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Diclofenac Sodium And Misoprostol (NDC 59762-0028). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Mylan Pharmaceuticals 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

Logo (Diclofenac 01)

FDA Label Image

Diclofenac 01a

FDA Label Image

Principal Display Panel (50 mg/200 mcg Tablet Bottle Label)

Principal Display Panel (50 mg/200 mcg Tablet Bottle Label)
Label for Greenstone Brand diclofenac sodium and misoprostol delayed-release tablets, 50 mg/200 mcg strength. The label states the product contains 60 tablets, is for oral use, and is distributed by Greenstone LLC. It includes storage instructions, a boxed warning about pregnancy, and has a barcode and 'Made in India' marking.*
FDA Label Image

Principal Display Panel (75 mg/200 mcg Tablet Bottle Label)

Principal Display Panel (75 mg/200 mcg Tablet Bottle Label)
Label for Greenstone brand diclofenac sodium and misoprostol delayed-release tablets, 75 mg/200 mcg, oral dosage form. The label indicates a 60 tablet count, with storage instructions at 20°C to 25°C, and a warning against use during pregnancy due to risk of miscarriage. The product is distributed by Greenstone LLC and made in India. The label includes a barcode and RX only notation.*

* 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.