Isosorbide Mononitrate Tablet
Product Images NDC 81665-103

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 Isosorbide Mononitrate (NDC 81665-103). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Omnivium Pharmaceuticals 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

Chemical Structure (Isosorbide Mononitrate Tablets Usp 1)

Chemical Structure (Isosorbide Mononitrate Tablets Usp 1)
Chemical structure diagram of isosorbide mononitrate showing its molecular arrangement, including oxygen, hydrogen atoms, and nitrate functional group.*
FDA Label Image

Label (Isosorbide Mononitrate Tablets Usp 2)

Label (Isosorbide Mononitrate Tablets Usp 2)
Isosorbide Mononitrate Tablets, USP 10 mg oral tablets label. The label includes dosage strength, quantity of 100 tablets, Rx only status, barcode, Omnivium Pharmaceuticals LLC as distributor, and storage instructions. The label also states each tablet contains 10 mg isosorbide mononitrate and advises to keep the container tightly closed.*
FDA Label Image

Label (Isosorbide Mononitrate Tablets Usp 3)

Label (Isosorbide Mononitrate Tablets Usp 3)
Label for Isosorbide Mononitrate Tablets, USP 20 mg, oral tablets distributed by Omnivium Pharmaceuticals LLC. The label indicates a package containing 100 tablets and includes storage instructions between 20° and 30°C (68° - 86°F). The product is identified with NDC 81665-103-10 and is marked Rx only.*

* 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.