Isosorbide Mononitrate Tablet, Extended Release
Product Images NDC 11788-160

8 FDA label images from Aiping Pharmaceutical, Inc. · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 8 technical images submitted to the FDA as part of the official labeling for Isosorbide Mononitrate (NDC 11788-160). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Aiping Pharmaceutical, 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

Isosorbide-structural Formula (Isosorbide Structural Formula)

Isosorbide-structural Formula (Isosorbide Structural Formula)
Chemical structure of Isosorbide Mononitrate showing its molecular framework with hydroxyl and nitrate ester functional groups.*
FDA Label Image

30 mg (100s)

30 mg (100s)
Label for Isosorbide Mononitrate Extended-Release Tablets, USP, 30 mg, produced by AiPing Pharmaceutical, Inc. The label indicates the product contains 100 tablets, each scored and oval-shaped, for oral use. Storage instructions specify 20° to 30°C. The label also includes a barcode, NDC 11788-159-01, and manufacturing details.*
FDA Label Image

30 mg (500s)

30 mg (500s)
Label for Isosorbide Mononitrate Extended-Release Tablets, USP, 30 mg, oral dosage form. The label indicates the product contains 500 tablets and is manufactured by AiPing Pharmaceutical, Inc. It includes storage instructions, dosage directions referencing the package insert, and a barcode.*
FDA Label Image

30 mg (1000s)

30 mg (1000s)
Label for Isosorbide Mononitrate Extended-Release Tablets, USP 30 mg by AiPing Pharmaceutical, Inc. The label specifies 1000 tablets, oral route, scorable oval-shaped tablets each containing 30 mg of isosorbide mononitrate. Storage instructions and dispensing information are included, along with the NDC 11788-159-10 and a barcode.*
FDA Label Image

60 mg (100s)

60 mg (100s)
Label for Isosorbide Mononitrate Extended-Release Tablets, USP, 60 mg, from AiPing Pharmaceutical, Inc. The label indicates the product contains 100 tablets, is prescription only, and includes storage instructions to keep at controlled room temperature (20° to 30°C). The label also includes dosage form as extended-release tablets and has a barcode with manufacturing and expiration details.*
FDA Label Image

60 mg (500s)

60 mg (500s)
Label for Isosorbide Mononitrate Extended-Release Tablets, USP, 60 mg, oral tablet by AiPing Pharmaceutical, Inc. The label indicates a package of 500 tablets, each scored capsule-shaped tablet contains 60 mg of isosorbide mononitrate. Storage instructions specify 20° to 30°C (68° to 86°F), and dispensing is recommended in tight containers. The label includes dosage advisory to see the package insert for full information, along with a barcode and spaces for GTIN, serial number, expiration, and lot number.*
FDA Label Image

60 mg (1000s)

60 mg (1000s)
Label for Isosorbide Mononitrate Extended-Release Tablets, USP 60 mg by AiPing Pharmaceutical, Inc., containing 1000 tablets. The label specifies the dosage form as extended-release tablets, capsule-shaped, each containing 60 mg active ingredient. Storage instructions and prescribing information references are included, along with a barcode and manufacturer details.*
FDA Label Image

120 mg (100s)

120 mg (100s)
Label for Isosorbide Mononitrate Extended-Release Tablets USP 120 mg by AiPing Pharmaceutical, Inc. The label states each oval-shaped tablet contains 120 mg of isosorbide mononitrate, includes storage instructions, and indicates a package size of 100 tablets. It also features a barcode and notes the product is Rx only.*

* 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.