Raloxifene Hydrochloride Tablet, Film Coated
Product Images NDC 65162-057

3 FDA label images from Amneal Pharmaceuticals Llc · 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 Raloxifene Hydrochloride (NDC 65162-057). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Amneal Pharmaceuticals 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.

Product Images & Figures Index

FDA Label Image

Chemical Structure (Raloxifene HCl Tablets Usp 1)

Chemical Structure (Raloxifene HCl Tablets Usp 1)
Chemical structure of raloxifene hydrochloride displayed as a 2D molecular diagram showing its key functional groups and bonds.*
FDA Label Image

Image 1 (Raloxifene HCl Tablets Usp 2)

Image 1 (Raloxifene HCl Tablets Usp 2)
Two line graphs showing total hip mean percentage change from baseline over 24 months after randomization. The first graph compares Raloxifene HCl and placebo groups across studies in North America and Europe. The second graph compares CE (conjugated estrogens), Raloxifene HCl, and placebo groups in a study of hysterectomized women. Both graphs display percentage change on the y-axis and months after randomization on the x-axis.*
FDA Label Image

1 (Raloxifene HCl Tablets Usp 3)

1 (Raloxifene HCl Tablets Usp 3)
Label for Raloxifene Hydrochloride Tablets, USP 60 mg, film-coated oral tablets. The label indicates the product is Rx only, with a quantity of 30 tablets. It is manufactured by Amneal Pharmaceuticals Pvt. Ltd and distributed by Amneal Pharmaceuticals LLC. The label includes storage instructions, a QR code, barcode, and a non-varnish area for lot and expiration date.*

* 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.