Entecavir Tablet
Product Images NDC 42494-457

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 42494-457). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Cameron Pharmaceuticals, 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

Chemical Structure (Entecavir 01)

Chemical Structure (Entecavir 01)
Chemical structure diagram of entecavir anhydrous, showing its molecular arrangement including hydroxyl groups, amino group, and the associated water molecule (hydrate). The stereochemistry is indicated by 4S, 3R, and 1S configurations in the cyclopentane ring.*
FDA Label Image

Principal Display Panel (0.5 mg Tablet Bottle Carton)

Principal Display Panel (0.5 mg Tablet Bottle Carton)
Packaging label for Entecavir tablets, USP 0.5 mg, a human prescription drug by Cameron Pharmaceuticals. The label indicates a package size of 30 tablets with NDC 42494-457-30. It includes storage instructions, child-resistant packaging information, and manufacturer details stating the product is made in China for Cameron Pharmaceuticals, Louisville, Kentucky.*
FDA Label Image

Principal Display Panel (1 mg Tablet Bottle Carton)

Principal Display Panel (1 mg Tablet Bottle Carton)
Carton label for Entecavir tablets, USP 1 mg, containing 30 tablets. The label includes the NDC 42494-458-30 and indicates the product is for prescription use only. Manufactured for Cameron Pharmaceuticals, Louisville, Kentucky. The label also provides storage instructions and a child-resistant warning. A barcode and revision date (April 2025) are present.*

* 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.