Disopyramide Phosphate Capsule, Gelatin Coated
Product Images NDC 59762-0386

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 Disopyramide Phosphate (NDC 59762-0386). 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

Chemical Structure (Disopyramide 01)

Chemical Structure (Disopyramide 01)
Chemical structure of disopyramide phosphate showing its molecular components including aromatic rings, functional groups, and the phosphate moiety.*
FDA Label Image

Logo (Disopyramide 02)

FDA Label Image

Principal Display Panel (100 mg Capsule Bottle Label)

Principal Display Panel (100 mg Capsule Bottle Label)
Label for Disopyramide Phosphate capsules USP, 100 mg strength, gelatin coated oral capsules. The label shows the NDC 59762-0386-1 and indicates a package size of 100 capsules. It displays the Greenstone® brand and states the product is distributed by Greenstone LLC in Peapack, NJ, made in Japan. Storage instructions and a dosage note about disopyramide base presence are included.*
FDA Label Image

Principal Display Panel (150 mg Capsule Bottle Label)

Principal Display Panel (150 mg Capsule Bottle Label)
Label for Disopyramide Phosphate capsules USP, 150 mg strength, gelatin coated, packaged in a container of 100 capsules. The product is identified as a Greenstone brand, prescription-only, distributed by Greenstone LLC, Peapack, NJ, and made in Japan. It includes storage instructions and mentions dosing information availability.*

* 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.