Nitroglycerin
Product Images NDC 67296-1775

Product Visual Gallery

This gallery contains 9 technical images submitted to the FDA as part of the official labeling for Nitroglycerin (NDC 67296-1775). 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

Carton1 (Carton1)

Packaging label for Nitroglycerin Sublingual Tablets USP 0.4 mg/tablet. The label shows the product name, strength, dosage form, and quantity of 4 bottles with 25 sublingual tablets each. It includes directions, storage instructions, and warnings. Manufactured by Ingenus Pharmaceuticals NJ, LLC and labeled for Dr. Reddy's Laboratories Inc.*

FDA Label Image

Carton2 (Carton2)

The packaging label for Nitroglycerin Sublingual Tablets, USP 0.3 mg/tablet, manufactured by RedPharm Drug. The label indicates storage instructions, warnings, and dosage notes, and states the package contains 100 sublingual tablets. The product NDC shown is 43598-435-01.*

FDA Label Image

Carton3 (Carton3)

Packaging label for Nitroglycerin Sublingual Tablets, USP 0.6 mg/tablet by Dr. Reddy's, distributed by RedPharm Drug. The label indicates the product contains 100 sublingual tablets, includes storage and dosage warnings, and advises patient package insert dispensing. The NDC shown is 43598-437-01.*

FDA Label Image

Carton4 (Carton4)

Packaging label for Nitroglycerin Sublingual Tablets, USP 0.4 mg by RedPharm Drug. The label includes dosage instructions, storage requirements at 20°-25°C, warnings about proper use and potency maintenance, and instructions not to crush, chew, or swallow the tablets. The package contains 100 sublingual tablets and indicates the product is prescription only.*

FDA Label Image

Container1 (Container1)

Nitroglycerin Sublingual Tablets, USP 0.4 mg per tablet packaging label showing 25 sublingual tablets. The label includes dosage strength and dispensing instructions. It is labeled for prescription use only and manufactured by Dr. Reddy's Laboratories, Inc. The label also includes a barcode, lot, and expiration date boxes.*

FDA Label Image

Container2 (Container2)

Label for Nitroglycerin Sublingual Tablets, USP, with a strength of 0.3 mg per tablet. The label states the product contains 100 sublingual tablets and is for prescription use only. It includes dosage, storage instructions, warnings against crushing or chewing the tablet, and manufacturer information including Dr. Reddy's Laboratories Inc. and Ingenus Pharmaceuticals NJ, LLC. The NDC number 43598-435-01 is printed at the top left.*

FDA Label Image

Container3 (Container3)

Label for Nitroglycerin Sublingual Tablets, USP 0.6 mg per tablet, containing 100 sublingual tablets. The label includes dosage and storage instructions, manufacturer and labeler information, and a barcode. The labeler is Dr. Reddy's Laboratories Inc. and the manufacturer is Incepta Pharmaceuticals NL, LLC.*

FDA Label Image

Container4 (Container4)

Label for Nitroglycerin Sublingual Tablets USP 0.4 mg/tablet, showing that the package contains 100 sublingual tablets. The label includes dosing instructions, storage information, warnings, manufacturing details by Humongous Pharmaceuticals NJ, LLC, and packaging by RedPharm Laboratories Inc. The label also features a barcode and notes the product is Rx only.*

FDA Label Image

Structure (Structure)

Chemical structure of Nitroglycerin showing the arrangement of nitrate groups attached to a glycerol backbone, along with its molecular formula C3H5N3O9 beneath the diagram.*

* 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.