Nitroglycerin
Product Images NDC 67296-1382

Product Visual Gallery

This gallery contains 9 technical images submitted to the FDA as part of the official labeling for Nitroglycerin (NDC 67296-1382). 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

Chemical Structure (Nitroglycerin 01)

Chemical structure of nitroglycerin showing the arrangement of nitrate groups attached to a three-carbon chain with oxygen atoms.*

FDA Label Image

Logo (Nitroglycerin 02)

Label showing Greenstone brand distributed by Greenstone LLC, Peapack, NJ 07977, under the labeler Redpharm Drug. The product proprietary name is NITROGLYCERIN, product NDC 67296-1382.*

FDA Label Image

Logo (Nitroglycerin 03)

Label for Greenstone brand Nitroglycerin distributed by Greenstone LLC, Peapack, NJ 07977. The label shows the Greenstone logo and distribution information from Redpharm Drug.*

FDA Label Image

Principal Display Panel (0.3 mg Tablet Bottle Label)

Label for Nitroglycerin sublingual tablets, USP, 0.3 mg per tablet, part of the Greenstone brand. The label indicates the tablets are for sublingual use, with 100 tablets in the package. It includes dosage and storage instructions, a warning to keep tablets tightly closed and out of reach of children, and specifies they should not be crushed, chewed, or swallowed. The label also shows the NDC 59762-4921-1 and the distributor Greenstone LLC, Peapack, NJ.*

FDA Label Image

Principal Display Panel (0.3 mg Tablet Bottle Carton)

Packaging label for Nitroglycerin sublingual tablets, USP, 0.3 mg per tablet, from the Greenstone brand. The label indicates 100 sublingual tablets and includes directions for dosage and use, storage instructions, barcode, and distributor information for Greenstone LLC. The label also features warnings about use and storage conditions.*

FDA Label Image

Principal Display Panel (0.4 mg Tablet Bottle Label)

Label for Nitroglycerin sublingual tablets, USP, 0.4 mg strength, from Redpharm Drug. The label indicates 100 sublingual tablets per container and includes dosage instructions, storage conditions, and a warning to keep the tablets in the original container and out of reach of children. It also includes handling instructions, manufacturer details, and an NDC number for patient packaging insert reference.*

FDA Label Image

Principal Display Panel (0.4 mg Tablet Bottle Carton)

Carton label for NITROGLYCERIN sublingual tablets, USP, 0.4 mg per tablet from Greenstone Brand. The label includes dosing and storage instructions, barcode and GTIN, and cautions about the tablet's 'burning or tingling' effect. The package contains 100 sublingual tablets distributed by Greenstone LLC.*

FDA Label Image

Principal Display Panel (0.6 mg Tablet Bottle Label)

Label for Nitroglycerin sublingual tablets USP, 0.6 mg per tablet, distributed by Greenstone LLC. The label advises storage at controlled room temperature and includes usage warnings to keep out of reach of children and not to crush, chew, or swallow the tablets. The package contains 100 sublingual tablets and is marked Rx only.*

FDA Label Image

Principal Display Panel (0.6 mg Tablet Bottle Carton)

Packaging label for Nitroglycerin sublingual tablets, USP, 0.6 mg per tablet by Greenstone Brand. The label includes instructions to dispense with patient package insert, storage information, dosage and use warnings, and barcode. The package contains 100 sublingual tablets and is distributed by Greenstone LLC.*

* 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.