Nitroglycerin Tablet
Product Images NDC 67296-2313

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 Nitroglycerin (NDC 67296-2313). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Redpharm Drug, 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 (Ce315fe7 2d3a 4c67 A2aa A026b770e10c 01)

Structure (Ce315fe7 2d3a 4c67 A2aa A026b770e10c 01)
Chemical structure of nitroglycerin, showing nitrogen dioxide (NO2) groups attached to a glycerin backbone with oxygen atoms connecting the functional groups.*
FDA Label Image

0.4mg 25 Bottle Label (Ce315fe7 2d3a 4c67 A2aa A026b770e10c 02)

0.4mg 25 Bottle Label (Ce315fe7 2d3a 4c67 A2aa A026b770e10c 02)
Nitroglycerin Sublingual Tablets, USP 0.4 mg/tablet label. The packaging includes a barcode, directions for pharmacists to dispense patient information separately, and storage instructions at 20°C to 25°C. The label also contains warnings against crushing, chewing, or swallowing sublingual tablets and advises storing tablets in the original container. Manufactured for Northstar Rx LLC, Memphis, TN, with a count of 25 sublingual tablets.*
FDA Label Image

0.4 mg Convenience Pack (Ce315fe7 2d3a 4c67 A2aa A026b770e10c 03)

0.4 mg Convenience Pack (Ce315fe7 2d3a 4c67 A2aa A026b770e10c 03)
Packaging label for Nitroglycerin Sublingual Tablets, USP 0.4 mg/tablet, supplied in a carton containing 4 bottles with 25 tablets each. The label shows the product name, strength, dosage form, manufacturer details, storage instructions, and a designated space for an RX label. The labeler is Redpharm Drug.*

* 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.