Isosorbide Mononitrate Tablet, Extended Release
Product Images NDC 0904-6449

4 FDA label images from Major Pharmaceuticals · 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 Isosorbide Mononitrate (NDC 0904-6449). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Major Pharmaceuticals, 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 (Chemical Structure)

Chemical-structure (Chemical Structure)
Chemical structure diagram of Isosorbide Mononitrate, showing its molecular framework with hydroxyl and nitrooxy functional groups.*
FDA Label Image
FDA Label Image

30mg Carton Label (34e0adcc 8899 4abb Bba4 6be95d0ce2dd 01)

30mg Carton Label (34e0adcc 8899 4abb Bba4 6be95d0ce2dd 01)
Packaging label for Isosorbide Mononitrate Extended-Release Tablets, USP 30 mg by Major Pharmaceuticals. The label indicates a unit dose package containing 100 tablets (10 x 10) with Rx only. Storage instructions and a note to keep out of reach of children are included, along with the NDC 0904-6449-61 and packaging details.*
FDA Label Image

60mg Carton Label (34e0adcc 8899 4abb Bba4 6be95d0ce2dd 00)

60mg Carton Label (34e0adcc 8899 4abb Bba4 6be95d0ce2dd 00)
Packaging label for Isosorbide Mononitrate Extended-Release tablets, 60 mg, by Major Pharmaceuticals. The label indicates a unit dose containing 100 tablets (10 x 10) with NDC 0904-6450-61. The product is oral, prescription-only, with storage instructions and warnings for institutional use with child-resistant closure.*

* 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.