Structure (Structure)
Chemical structure diagram of nitroglycerin with its molecular formula C3H5N3O9 shown below the structure.*
Nitroglycerin Tablet
Product Images NDC 43598-437
9 FDA label images from Dr. Reddys Laboratories Inc · Packaging, Regulatory Labels, and Product Appearance
Product Visual Gallery
This gallery contains 9 technical images submitted to the FDA as part of the official labeling for Nitroglycerin (NDC 43598-437). 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.
Product Images & Figures Index
Carton 1 (0.3 mg 100 Tab Carton)
Packaging label for Nitroglycerin Sublingual Tablets, USP 0.3 mg per tablet by Dr. Reddys Laboratories Inc. The label includes dosage form as sublingual tablets, storage instructions (20°-25°C), warnings, and directions to keep out of children’s reach. It indicates a package size of 100 sublingual tablets and states 'Rx Only' with no varnish measurements printed in orange on the side.*
Container 1 (0.3 mg 100 Tab Container)
The label for Nitroglycerin Sublingual Tablets, USP, 0.3 mg per tablet, shows the dosage form as sublingual tablets with a package size of 100 tablets. The label includes dosage instructions, storage warnings, and manufacturer information for Dr. Reddys Laboratories Inc. It also specifies the product as prescription only (Rx Only) and features the NDC code 43598-435-01.*
Container 2-1 (0.4 mg 25 Tab Container)
Label for Nitroglycerin Sublingual Tablets, USP 0.4 mg per tablet, containing 25 sublingual tablets. The label includes dosage and storage instructions, warnings, and manufacturer information from Dr. Reddys Laboratories Inc. The label is designed with clear identification of the active ingredient strength and dispensing instructions for prescription use only.*
Carton 2-1 (0.4 mg 25 Tab Carton)
Packaging label for Nitroglycerin Sublingual Tablets USP 0.4 mg per tablet by Dr. Reddy's Laboratories Inc. The label indicates sublingual tablets with a package count of 4 bottles of 25 tablets each. The label includes dosage strength, directions to dispense with the patient package insert, storage conditions, usage notes, and manufacturers' details. Barcode and NDC 43598-436-11 are visible.*
Container-3 (0.6 mg 100 Tab Container)
Label for Nitroglycerin Sublingual Tablets USP, 0.6 mg per tablet, by Dr. Reddys Laboratories Inc. The label states 100 sublingual tablets, with storage instructions at 20-25°C and warnings about keeping tablets out of reach of children and not crushing or chewing them. It includes prescribing and potency loss warnings, barcode, and lot/expiration placeholders.*
Carton 3 (0.6 mg 100 Tab Carton)
Packaging label for Nitroglycerin Sublingual Tablets, USP 0.6 mg per tablet, manufactured by Dr. Reddys Laboratories Inc. The label indicates 100 tablets per package, with storage instructions at 20°-25°C (68°-77°F). The label includes warnings to keep out of reach of children, not to crush or chew, and to close tightly after use.*
Container 2-2 (0.4 mg 100 Tab Container)
Nitroglycerin Sublingual Tablets USP label showing 0.4 mg strength per tablet. The label indicates 100 sublingual tablets in the package, marked for prescription use only. It includes dosage and storage instructions, warns to keep out of reach of children, and advises to use sublingual tablets without crushing, chewing, or swallowing. Labeler is Dr. Reddys Laboratories Inc.*
Carton 2-2 (0.4 mg 100 Tab Carton)
Nitroglycerin Sublingual Tablets USP 0.4 mg per tablet packaging label by Dr. Reddys Laboratories Inc. The carton states the product contains 100 sublingual tablets and includes storage instructions to keep at controlled room temperature (20°-25°C). It warns against crushing, chewing, or swallowing the tablets and emphasizes dispensing with patient package insert. The label also notes usual dosage directions should follow prescribing information and cautions about possible sensations during use.*
* 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.
