Niacin Tablet, Film Coated, Extended Release
Product Images NDC 47335-614

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Niacin (NDC 47335-614). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Sun Pharmaceutical Industries, 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

Niacin-structure (Niacin Structure)

Chemical structure of niacin, showing a pyridine ring with a carboxyl group. Also included are the molecular formula C6H5NO2 and molecular weight 123.11.*

FDA Label Image

Spl Label 1000mg

Label for Niacin Extended-Release Tablets, USP, 1000 mg film-coated tablets. The label indicates a prescription drug distributed and manufactured by Sun Pharmaceutical Industries, Inc., with a package size of 90 tablets. Storage instructions and pharmacist dispensing information are also included, along with a barcode and the Sun Pharma logo.*

FDA Label Image

Spl Label 500mg

Label for Niacin Extended-Release Tablets, USP, 500 mg film-coated extended-release tablets. The label indicates a package count of 90 tablets, distributed by Sun Pharmaceutical Industries, Inc. It includes dosage and storage instructions and features the Sun Pharma logo.*

FDA Label Image

Spl Label 750mg

Label for Niacin Extended-Release Tablets, USP 750 mg, film-coated, extended release oral tablets. The label includes storage instructions, dosage reference, and child-resistant container requirement. Distributed by Sun Pharmaceutical Industries, Inc., and manufactured by Sun Pharmaceutical Industries Limited. The package contains 90 tablets with the NDC 47335-614-81.*

* 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.