Voriconazole Tablet, Film Coated
Product Images NDC 16714-199

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Voriconazole (NDC 16714-199). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Northstar Rx Llc, 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

Package Label-principal Display Panel (50 mg (30 Tablet Bottle))

Each tablet of Voriconazole USP contains 50 mg. It is a film-coated tablet and should be stored within the temperature range of 20 to 25°C. The tablets should be dispensed in tight containers and stored in controlled room temperature as per USP guidelines. Manufacturing dated 10/2021, the product is from India by Aurobindo Pharma Limited and is bottled in 30 tablets per bottle. Dosage and usage information can be found in the prescribing information. All the necessary information including NDC and M.L No. are provided.*

FDA Label Image

Package Label-principal Display Panel (200 mg (30 Tablet Bottle))

This is a description of Voriconazole USP 200 mg film-coated tablets, which come in bottles of 30 tablets made in India. The tablets are dispensed in tight containers, and users should refer to the included prescribing information for dosage and use. The NDC code for the tablets is 16714-199-01, and the Manufacturing License Number is 22/MN/AP/2009/F/R. The tablets were manufactured for Northstar RxLLC by Aurobindo Pharma Limited, and they should be kept in a cool and dry place.*

FDA Label Image

Chemical Structure (Voriconazole Str)

* 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.