Raloxifene Hydrochloride Tablet
Product Images NDC 69097-825

3 FDA label images from Cipla Usa Inc. · 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 69097-825). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Cipla Usa Inc., 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

Raloxifene Hydrochloride Tablets 60 mg

Raloxifene Hydrochloride Tablets 60 mg
Packaging label for Raloxifene Hydrochloride Tablets, USP 60 mg by Cipla USA Inc. The label indicates 30 tablets per container, prescription only, with storage instructions at 20°-25°C. Manufactured by InvaGen Pharmaceuticals, Inc., a Cipla subsidiary, with lot, expiration, and barcode visible on the label.*
FDA Label Image

Raloxifene Hydrochloride Str

Raloxifene Hydrochloride Str
Chemical structure diagram of Raloxifene, the active ingredient in Raloxifene Hydrochloride 60 mg oral tablets by Cipla USA Inc. The diagram shows molecular rings and functional groups representative of Raloxifene, including a chloride ion (Cl-) associated with the structure.*
FDA Label Image

Raloxifene Graph

Raloxifene Graph
Two line graphs showing total hip mean percentage change from baseline over 24 months post-randomization. The top graph compares Raloxifene and Placebo groups, showing Raloxifene with an increase in percentage change, while Placebo remains near zero or negative. The bottom graph compares CE (conjugated estrogens), Raloxifene, and Placebo in hysterectomized women, with CE showing the greatest increase, Raloxifene a moderate increase, and Placebo a decrease.*

* 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.