Nitroglycerin Tablet
Product Images NDC 69339-174

Product Visual Gallery

This gallery contains 9 technical images submitted to the FDA as part of the official labeling for Nitroglycerin (NDC 69339-174). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Natco Pharma Usa 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

Carton-0-3mg (0 3 mg Carton)

Packaging label for Nitroglycerin Sublingual Tablets, USP 0.3 mg/tablet by Natco Pharma USA LLC. The label shows a bottle carton containing 1 x 100 sublingual tablets, prescription-only. It includes dosage instructions, storage conditions, warnings about the sensation upon use, and manufacturer information along with barcodes and the NDC 69339-173-01.*

FDA Label Image

Label 0-3mg (0 3mg Label)

Nitroglycerin Sublingual Tablets, USP, 0.3 mg per tablet, packaged by Natco Pharma USA LLC. The label indicates a prescription-only sublingual tablet form with a count of 100 tablets per bottle. It includes dosage instructions, warnings, storage conditions, and manufacturer details, featuring barcodes and lot information on the label.*

FDA Label Image

Carton-0-4mg (0 4mg Carton)

Packaging label for Nitroglycerin Sublingual Tablets, USP 0.4 mg per tablet, manufactured by Natco Pharma USA LLC. The package contains 100 sublingual tablets, with dosage instructions and storage information. It includes warnings about potential sensations and advises keeping tablets in the original container, along with distributor details from DASH Pharmaceuticals LLC.*

FDA Label Image

Label 0-4mg (0 4mg Label)

Nitroglycerin Sublingual Tablets, USP 0.4 mg/tablet in a carton labeled for Rx only. The package contains 1 x 100 sublingual tablets. The label includes dosage instructions, storage conditions, warnings about proper use, and manufacturer details: Natco Pharma USA LLC. The label also shows a barcode and blanks for the lot number and expiration date.*

FDA Label Image

Label 0-4mg 25 (0 4mgx25label)

NITROGLYCERIN Sublingual Tablets USP 0.4 mg per tablet, packaged as 25 sublingual tablets. The label includes NDC 69339-174-02, instructions for storage at 20° to 25°C, usual dosage advisory, and warnings about handling and potency. It is labeled for prescription use only by Natco Pharma USA LLC and manufactured by DASH Pharmaceuticals LLC.*

FDA Label Image

Carton-4x25 0-4mg (0 4x25mg Carton)

Packaging label for Nitroglycerin Sublingual Tablets, USP 0.4 mg per tablet. The label states a package size of 4 x 25 sublingual tablets. It is labeled Rx only and includes handling information for pharmacists and patients. The product is manufactured by Natco Pharma Limited, India, and distributed by DASH Pharmaceuticals, USA.*

FDA Label Image

Carton-0-6mg (0 6mg Carton)

Label for Nitroglycerin Sublingual Tablets, USP 0.6 mg/tablet in a carton containing 1 x 100 sublingual tablets. The label shows the proprietary name Nitroglycerin and strength prominently, with instructions to dispense accompanying patient information. Manufactured by Natco Pharma USA LLC and produced by Natco Pharma Limited, India. Packaging includes storage instructions and a barcode.*

FDA Label Image

Label 0-6mg (0 6mg Label)

NITROGLYCERIN Sublingual Tablets, USP, 0.6 mg per tablet, in a package labeled for prescription use only. Manufactured by Natco Pharma USA LLC, the label includes dosing instructions, storage conditions, and warnings about the medication. The packaging shows a lot number and expiration date area, with barcodes and regulatory information.*

FDA Label Image

Structure (Structure)

Chemical structure of nitroglycerin (C3H5N3O9), showing the molecular arrangement with nitro groups attached to a glycerin backbone.*

* 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.