Tamoxifen Citrate Tablet, Film Coated
Product Images NDC 59651-300

3 FDA label images from Aurobindo Pharma Limited · 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 Tamoxifen Citrate (NDC 59651-300). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Aurobindo Pharma Limited, these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.

Product Images & Figures Index

FDA Label Image

Package Label-principal Display Panel (10 mg)

Package Label-principal Display Panel (10 mg)
Tamoxifen Citrate Tablets, USP 10 mg film-coated tablets label by Aurobindo Pharma USA, Inc. The label states the package contains 60 tablets. It includes dosage strength information, storage instructions at 20° to 25°C, and dispensing guidelines. The label notes each tablet contains 15.2 mg tamoxifen citrate, equivalent to 10 mg tamoxifen, and includes a barcode and manufacturer details.*
FDA Label Image

Package Label-principal Display Panel (20 mg)

Package Label-principal Display Panel (20 mg)
Tamoxifen Citrate Tablets, USP 20 mg film-coated oral tablets in a unit-of-use container labeled for 30 tablets. The label includes dosage strength, storage instructions, warning to keep out of reach of children, and distribution details by Aurobindo Pharma USA, Inc. Manufactured in India by Aurobindo Pharma Limited.*
FDA Label Image

Chemical Structure (Tamoxifen Str)

Chemical Structure (Tamoxifen Str)
Chemical structure diagram of Tamoxifen Citrate showing the molecular formula C32H37NO8 with labeled chemical groups attached to the core structure.*

* 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.