Raloxifene Hydrochloride
Product Images NDC 71335-1663

3 FDA label images from Bryant Ranch Prepack · 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 71335-1663). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Bryant Ranch Prepack, 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

Image (Raloxifene Hydrochloride Str)

Image (Raloxifene Hydrochloride Str)
Chemical structure diagram of the active ingredient in Raloxifene Hydrochloride, showing the molecular arrangement including aromatic rings, a chloride ion, and hydroxyl groups.*
FDA Label Image

Image (Raloxifene Graph)

Image (Raloxifene Graph)
This figure contains two line graphs showing the total hip mean percentage change from baseline over 24 months after randomization. The first graph compares placebo and raloxifene subjects from studies NA and EU, while the second graph includes placebo, raloxifene, and conjugated estrogens (CE) subjects from study INT (hysterectomized women). Both graphs depict changes in hip bone mineral density percentages over time with corresponding error bars.*
FDA Label Image

Label Image (Lbl713351663)

Label Image (Lbl713351663)
Raloxifene 60 mg tablet packaging label from Bryant Ranch Prepack. The label includes storage instructions to keep at room temperature between 20°-25°C (68°-77°F), a comparison to Evista 60 mg tablet by InvaGen Pharmaceuticals, and a package count of 60 tablets. The label also features a barcode and a caution to keep drugs out of children's reach.*

* 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.