Entecavir Tablet, Film Coated
Product Images NDC 16714-718

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 Entecavir (NDC 16714-718). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Northstar Rxllc, 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

2fd6b7bb 29c2 4f25 Bd96 33b64fdfefdb 01

2fd6b7bb 29c2 4f25 Bd96 33b64fdfefdb 01
Chemical structure of entecavir monohydrate, showing the molecular arrangement of atoms including nitrogen, carbon, oxygen, and hydrogen in the compound.*
FDA Label Image

2fd6b7bb 29c2 4f25 Bd96 33b64fdfefdb 02

2fd6b7bb 29c2 4f25 Bd96 33b64fdfefdb 02
Label for Entecavir 0.5 mg film-coated tablets, USP, displaying the NDC number 16714-717-01. The label states the product contains 30 tablets and is manufactured for NorthStar Rx LLC. Storage instructions and manufacturing details (by Cipla Ltd., India) are included. A barcode and a designated area for batch overprinting with GTIN, serial number, expiry, and lot are also visible.*
FDA Label Image

2fd6b7bb 29c2 4f25 Bd96 33b64fdfefdb 03

2fd6b7bb 29c2 4f25 Bd96 33b64fdfefdb 03
Label for Entecavir 1 mg film-coated tablets, USP, containing 30 tablets per bottle. The label shows the product name 'Entecavir', strength '1 mg', and 'Tablets, USP'. It indicates prescription use only (Rx only) and lists NorthStar Rx LLC as the labeler, with manufacturing by Cipla Ltd. in India. Storage instructions and typical batch information areas for GTIN, serial number, expiry, and lot are included.*

* 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.