Niacin
Product Images NDC 68180-221
View Photos of Packaging, Regulatory Labels, and Product Appearance
Product Visual Gallery
This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Niacin (NDC 68180-221). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.
As provided by Lupin Pharmaceuticals, 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.
D0cd43a4 3390 4e2f Bd9f D907b4710071 02
This is a medication called Niacin Extended-release Tablets USP manufactured by Lupin Pharmaceuticals. Each tablet contains 500mg niacin USP. The usual dosage should be determined by a prescribing physician. The pharmacist must dispense the patient information leaflet separately to each customer purchasing this medication. The tablets should be stored at a controlled room temperature between 15-30°C (59-86°F) in a container with a child-resistant cap. It was manufactured in India and distributed in Baltimore, MD, USA.*
D0cd43a4 3390 4e2f Bd9f D907b4710071 03
This is a medication produced by Lupin Pharmaceuticals containing 750 mg of niacin. The medication is in the form of a film-coated extended-release tablet, and users should refer to the prescribing information for dosage instructions. The tablets should be kept in a tightly sealed container with a child-resistant closure at a temperature between 15 to 30°C (59-86°F). The medication is only available through a prescription from a qualified healthcare practitioner. A patient information leaflet is provided separately to each patient, and each package contains 100 tablets.*
D0cd43a4 3390 4e2f Bd9f D907b4710071 04
This is a description of a medication called "Niacin Extended-release Tablets USP". The medication comes in a bottle containing 100 tablets, and each film-coated extended-release tablet contains niacin USP at a strength of 1000 mg. The prescribing information should be consulted for the usual dosage. The tablets should be dispensed in a tight container with child-resistant closure and stored at controlled room temperature. The medication is distributed and manufactured by Lupin Pharmaceuticals in the United States and Lupin Limited in Goa, India. The text also contains the product code, NDC number, and a request for the pharmacist to dispense the patient information leaflet provided separately to each patient.*
* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.