Niacin Tablet, Extended Release
Product Images NDC 62175-320

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Niacin (NDC 62175-320). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Lannett Company, 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

Structure Formula (Niacin Extended Release Tablets Usp 1)

Structure Formula (Niacin Extended Release Tablets Usp 1)
Chemical structure of Niacin (nicotinic acid), showing a pyridine ring with a carboxyl group (COOH) attached. The molecular formula is C6H5NO2 with a molecular weight of 123.11.*
FDA Label Image

500 mg 90 Count Bottle Label (Niacin Extended Release Tablets Usp 2)

500 mg 90 Count Bottle Label (Niacin Extended Release Tablets Usp 2)
Label for Niacin Extended-release Tablets, USP 500 mg oral tablets. The label indicates each film-coated tablet contains 500 mg of niacin in extended-release form. The package contains 90 tablets. It is distributed by Lannett Company, Inc., Philadelphia, PA. Storage instructions and dispensing cautions are also present along with a barcode and NDC 62175-320-46.*
FDA Label Image

1000 mg 90 Count Bottle Label (Niacin Extended Release Tablets Usp 3)

1000 mg 90 Count Bottle Label (Niacin Extended Release Tablets Usp 3)
Label of Niacin Extended-release Tablets, USP 1000 mg with 90 tablets per bottle. The label includes warnings about the seal, storage instructions (20° to 25°C), and directs users to package inserts for dosage information. Distributed by Lannett Company, Inc., Philadelphia, PA. The label features the NDC 62175-322-46 and a barcode.*

* 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.