Nitroglycerin Tablet
Product Images NDC 59651-658

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 7 technical images submitted to the FDA as part of the official labeling for Nitroglycerin (NDC 59651-658). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Aurobindo Pharma Limited, 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

Package Label-principal Display Panel (0.3 mg (100 Tablets Bottle))

Package Label-principal Display Panel (0.3 mg (100 Tablets Bottle))
Packaging label for Nitroglycerin Sublingual Tablets, USP 0.3 mg per tablet by Aurobindo Pharma Limited. The label shows 100 sublingual tablets with prescription-only status. It includes dosage strength, barcode, storage instructions, warnings, and manufacturer information stating the product is made in India and distributed by Aurobindo Pharma USA.*
FDA Label Image

Package Label-principal Display Panel (0.3 mg (100 Tablets Carton))

Package Label-principal Display Panel (0.3 mg (100 Tablets Carton))
Packaging label for Nitroglycerin Sublingual Tablets, USP 0.3 mg/tablet by Aurobindo Pharma Limited. The label shows the product name, strength, dosage form, quantity (100 sublingual tablets), and NDC 59651-657-00. The label includes usage instructions, storage conditions, and manufacturer contact information.*
FDA Label Image

Package Label-principal Display Panel (0.4 mg (25 Tablets Bottle))

Package Label-principal Display Panel (0.4 mg (25 Tablets Bottle))
Packaging label for Nitroglycerin Sublingual Tablets USP 0.4 mg per tablet, with a quantity of 25 sublingual tablets. The label shows distribution by Aurobindo Pharma USA, Inc., made in India. It includes dosage and storage instructions, patient information URL, lot and expiration placeholders, and gluing areas for packaging assembly.*
FDA Label Image

Package Label-principal Display Panel (0.4 mg (4x25 Tablets Carton))

Package Label-principal Display Panel (0.4 mg (4x25 Tablets Carton))
Carton label for Nitroglycerin Sublingual Tablets USP, 0.4 mg per tablet, supplied by Aurobindo Pharma Limited. The label shows the product name, strength, dosage form (sublingual tablets), package size (4 bottles x 25 tablets), and usage as prescription only. The label includes storage and warning information, barcodes, and branding.*
FDA Label Image

Package Label-principal Display Panel (0.6 mg (100 Tablets Bottle))

Package Label-principal Display Panel (0.6 mg (100 Tablets Bottle))
Packaging label for Nitroglycerin Sublingual Tablets USP 0.6 mg/tablet from Aurobindo Pharma Limited. The label indicates a package of 100 sublingual tablets with instructions to keep them in the original container and warnings against crushing, chewing, or swallowing. Storage conditions and distributor information (Aurobindo Pharma USA, Inc.) are included.*
FDA Label Image

Package Label-principal Display Panel (0.6 mg (100 Tablets Carton))

Package Label-principal Display Panel (0.6 mg (100 Tablets Carton))
Packaging label for Nitroglycerin Sublingual Tablets, USP 0.6 mg/tablet by Aurobindo Pharma Limited. The label displays the product name, strength, dosage form, quantity of 100 sublingual tablets, and NDC 59651-659-00. It includes dosage and usage instructions, storage conditions, and distributor details. The label also features barcodes and a 2D data matrix area for batch information.*
FDA Label Image

Chemical Structure (Nitroglycerin Str)

Chemical Structure (Nitroglycerin Str)
Chemical structure of nitroglycerin (C3H5N3O9) depicted as a nitrate ester with three nitrate groups attached to a glycerol 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.