Raloxifene Hydrochloride Tablet, Film Coated
Product Images NDC 0904-6902

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 Raloxifene Hydrochloride (NDC 0904-6902). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Major 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.

Product Images & Figures Index

FDA Label Image

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Raloxifene hydrochloride 60 mg film-coated tablets label from Major Pharmaceuticals. The label includes product and dosage information, package count of 30 tablets, and instructions for pharmacist dispensing with medication guide. It also displays storage conditions, manufacturer details, and the NDC 0904-6902-04.*
FDA Label Image

Figure 1: Total Hip Bone Mineral Density Mean Percentage Change From Baseline (Raloxifene Pi 02v1)

Figure 1: Total Hip Bone Mineral Density Mean Percentage Change From Baseline (Raloxifene Pi 02v1)
Two line graphs depicting total hip mean percentage change from baseline over 24 months after randomization. The first compares Raloxifene versus placebo in all placebo and Raloxifene subjects from studies in North America and Europe. The second compares placebo, Raloxifene, and conjugated estrogens (CE) in hysterectomized women, showing percentage change trends across the same timeline.*
FDA Label Image

Chemical Structure (Raloxifene Pi)

Chemical Structure (Raloxifene Pi)
Chemical structure of raloxifene hydrochloride, illustrating the molecular arrangement including aromatic rings, hydroxyl groups, and a hydrochloride ion (Cl-). This structure depicts the active ingredient raloxifene hydrochloride.*

* 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.