Diclofenac Sodium And Misoprostol Tablet, Film Coated
Product Images NDC 59762-0029

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 59762-0029). 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)

The text suggests that there is a brand called "GREENSTONE®" that is distributed by a company called "Greenstone LLC" located in NJ 07977.*

FDA Label Image

Diclofenac 01a

This text appears to be the brand name and distributor information for Greenstone LLC based in Peapack, NJ. Greenstone LLC may potentially distribute a variety of products under the Greenstone® brand.*

FDA Label Image

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

This text provides storage instructions for diclofenac sodium and misoprostol delayed-release tablets. It also includes dosage and use information. The tablets contain diclofenac sodium and misoprostol, with each tablet containing 50 mg and 200 mcg, respectively. The medication should be dispensed in child-resistant containers and with a medication guide. The manufacturer of the medication is Greenstone, located in Peapack, NJ. The Global Trade Identification Number (GTIN) is 00359762002815.*

FDA Label Image

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

Store the delayed-release tablets of diclofenac sodium and misoprostol at room temperature between 20°C to 25°C (68°F to 77°F) with permitted excursions between 15°C to 30°C (59°F to 86°F). The tablets should be dispensed in USP tight, child-resistant containers. Each tablet contains 75 mg of diclofenac sodium and 200 micrograms of misoprostol. For dosage and usage, refer to the accompanying prescribing information. These Greenstone brand tablets are made in India and should always be dispensed with a medication guide. The product is distributed by Grocnsione 110 Peapack, N3 07577 and the NDC number is 59762-0029-1.*

* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.