Isosorbide Dinitrate Tablet
Product Images NDC 16714-008

Product Visual Gallery

This gallery contains 5 technical images submitted to the FDA as part of the official labeling for Isosorbide Dinitrate (NDC 16714-008). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Northstar Rx 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

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Chemical structure of isosorbide dinitrate showing its molecular connectivity with nitrooxy groups attached to the isosorbide backbone.*

FDA Label Image

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Label for Isosorbide Dinitrate Tablets USP 5 mg oral tablets, packaged in a bottle of 100 tablets. The label shows the NDC 16714-007-01 and indicates the product is prescription only. It includes storage instructions, manufacturer information: Northstar Rx LLC, Memphis, TN, and Cadila Healthcare Ltd., India, plus a barcode.*

FDA Label Image

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Isosorbide Dinitrate Tablets USP 10 mg oral tablets label in a 100-tablet package. The label states the active ingredient strength, manufacturer Northstar Rx LLC, and manufacturer Cadila Healthcare Ltd., India. Storage instructions and standard cautions to keep the drug out of reach of children are also included.*

FDA Label Image

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Isosorbide Dinitrate Tablets, USP 20 mg oral tablet label from Northstar Rx LLC. The label states a package count of 100 tablets. It includes storage instructions to keep between 20° to 25°C, protect from light, and keep tightly closed in a light-resistant container. Manufactured by Cadila Healthcare Ltd., India. The label also features the NDC code 16714-009-01.*

FDA Label Image

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The label for Isosorbide Dinitrate Tablets, USP, 30 mg, oral tablets features a white and blue color scheme with green highlighting the strength. The label states it contains 100 tablets, with the manufacturer as Cadila Healthcare Ltd., India, and the labeler Northstar Rx LLC. The NDC is 16714-010-01. Storage and safety instructions are included.*

* 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.