Nitroglycerin Tablet
Product Images NDC 43598-436

Product Visual Gallery

This gallery contains 9 technical images submitted to the FDA as part of the official labeling for Nitroglycerin (NDC 43598-436). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Dr. Reddys Laboratories Inc, 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

Carton1 (Carton1)

Packaging label for Nitroglycerin Sublingual Tablets USP 0.4 mg per tablet. The carton indicates this is a prescription drug containing sublingual tablets, with a quantity of 4 bottles each containing 25 tablets. It includes storage instructions and warnings. Manufactured for Dr. Reddy's Laboratories Inc. by Ingenus Pharmaceuticals NJ, LLC.*

FDA Label Image

Carton2 (Carton2)

Packaging label for Nitroglycerin Sublingual Tablets, USP 0.3 mg per tablet, manufactured by Dr. Reddys Laboratories Inc. The label indicates this is a prescription drug with 100 sublingual tablets per container. Storage instructions and usage warnings are provided, including dosage caution and tablet handling advice.*

FDA Label Image

Carton3 (Carton3)

Packaging label for Nitroglycerin Sublingual Tablets, USP 0.6 mg per tablet by Dr. Reddys Laboratories Inc. The label includes dosage form as sublingual tablets and instructs to always dispense with patient package insert. It contains usual dosage and warning information, storage instructions (20°-25°C/68°-77°F), and cautions against crushing, chewing, or swallowing tablets. The package contains 100 sublingual tablets and includes an NDC barcode.*

FDA Label Image

Carton4 (Carton4)

Nitroglycerin Sublingual Tablets, USP 0.4 mg per tablet in a carton designed for 100 sublingual tablets. The label includes dosage strength, storage instructions, and a warning to keep the medication in its original container and out of children's reach. The product is manufactured by Dr. Reddys Laboratories Inc and is labeled for prescription use only.*

FDA Label Image

Container1 (Container1)

Packaging label for Nitroglycerin Sublingual Tablets, USP, 0.4 mg per tablet, by Dr. Reddys Laboratories Inc. The label indicates it contains 25 sublingual tablets, with prescription-only status. It includes dosing and safety information, the NDC 43598-436-35, and barcode details.*

FDA Label Image

Container2 (Container2)

Label for Nitroglycerin Sublingual Tablets USP, 0.3 mg per tablet, manufactured by Dr. Reddys Laboratories Inc. The label indicates a quantity of 100 sublingual tablets. It includes dosage instructions, storage information, and safety warnings such as avoiding crushing or chewing the tablets and keeping out of reach of children.*

FDA Label Image

Container3 (Container3)

Label for Nitroglycerin Sublingual Tablets, USP 0.6 mg/tablet by Dr. Reddys Laboratories Inc. The label indicates a package containing 100 sublingual tablets, with instructions to always dispense with patient package insert. Storage instructions and manufacturing details by Ingress Pharmaceuticals NL LLC and Dr. Reddys Laboratories Inc. in Princeton, NJ are also shown.*

FDA Label Image

Container4 (Container4)

Label for Nitroglycerin Sublingual Tablets, USP 0.4 mg per tablet by Dr. Reddys Laboratories Inc. The label indicates 100 sublingual tablets per container with instructions to always dispense with a patient package insert. It includes storage instructions, warnings, dosage guidelines, and manufacturer information along with a barcode and NDC 43598-436-01.*

FDA Label Image

Structure (Structure)

Chemical structure diagram of nitroglycerin with its molecular formula C3H5N3O9 shown below the structure.*

* 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.