Niacin
Product Images NDC 50268-586

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Niacin (NDC 50268-586). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Avpak, 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

1 (Screen Shot 2017 09 14 At 1.17.14 Pm)

This is a medication with the brand name Niacin, which is a type of vitamin B3. It comes as an extended-release tablet in the strength of 500mg. The medication is available in a package of 30 tablets with three unit doses of ten tablets each, and it is prescribed only with a valid medical prescription. The tablets are film-coated and contain niacin, USP 500mg. The medication information is provided separately. It should be kept at a controlled room temperature of 20° to 25°C (68° to 77°F) and away from children. It is a product of Avkare, Inc., and the manufacturing location is in Pulaski, TN 38478.*

FDA Label Image

2 (Screen Shot 2017 09 14 At 1.17.30 Pm)

This is a description of a medication with the NDC code 50268-586-13. The medication contains 1000mg of Niacin per film-coated extended-release tablet. The tablet is meant to be taken as prescribed, and comes in a unit dose of 30 tablets. This medication is only available with a prescription, as denoted by "Rx Only" in the text. The instructions for use can be found in the package insert. The medication should be stored at a controlled room temperature between 20 and 25°C. The medication is manufactured for AVKARE, Inc. located in Pulaski, TN. There is a revision date of 07-2015-01 and "AV 0317" printed on the label.*

FDA Label Image

4097803e-figure-01 (Niacin Extended Release Tablets 500 mg 1000 mg 1)

* 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.