Isosorbide Mononitrate
Product Images NDC 71610-337

Product Visual Gallery

This gallery contains 5 technical images submitted to the FDA as part of the official labeling for Isosorbide Mononitrate (NDC 71610-337). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Aphena Pharma Solutions - Tennessee, 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

Structure (6b9ba49c 9475 48db 8dc1 6a99631f8535 01)

Chemical structure of Isosorbide Mononitrate, showing the molecular configuration with oxygen, hydrogen, and nitrate groups.*

FDA Label Image

Bottle Label 120 mg (71610 0321 05)

Packaging label for Isosorbide Mononitrate ER, USP 120 mg, containing 4200 tablets. The label includes storage instructions, manufacturer information (RA Chem Pharma Limited, Hyderabad, India), and repackager details (Aphena Pharma Solutions - Tennessee, LLC). It also notes the product is prescription only.*

FDA Label Image

Bottle Label 60 mg (71610 0337 30)

Packaging label for Isosorbide Mononitrate ER, USP 60 mg tablets, supplied in a bottle of 30 tablets. The label shows storage instructions, manufacturer as RA Chem Pharma Limited in Hyderabad, India, and labeler as Aphena Pharma Solutions - Tennessee, LLC.*

FDA Label Image

Bottle Label 30 mg (71610 0338 30)

Packaging label for Isosorbide Mononitrate ER, USP, 30 mg tablets. The label indicates a quantity of 30 tablets and specifies storage instructions between 20-25 degrees Celsius. Manufactured by RA Chem Pharma Limited in Hyderabad, India, and packed by Aphena Pharma Solutions - Tennessee, LLC in Cookeville, TN. The label includes a barcode and regulatory information such as the NDC number.*

FDA Label Image

Aphena Pharma Solutions (TN)

* 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.