Duavee Tablet, Film Coated
Product Images NDC 63539-122

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 6 technical images submitted to the FDA as part of the official labeling for Duavee (NDC 63539-122). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by U.s. 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.

FDA Label Image

Chemical Structure (Duavee 01)

Chemical Structure (Duavee 01)
Chemical structure of bazedoxifene acetate, a component of the conjugated estrogens/bazedoxifene combination product Duavee.*
FDA Label Image

Logo (Duavee 02)

FDA Label Image

Duavee 02a

FDA Label Image

Principal Display Panel (15 Tablet Blister Card)

Principal Display Panel (15 Tablet Blister Card)
Duavee 0.45 mg/20 mg tablet packaging label showing conjugated estrogens/bazedoxifene film-coated tablets. The label indicates 7 tablets per foil pouch, with storage instructions, prescribed use information, and distribution by U.S. Pharmaceuticals and Pfizer Inc. The label notes the product is a professional sample and not for sale.*
FDA Label Image

Principal Display Panel (7 Tablet Blister Pouch)

Principal Display Panel (7 Tablet Blister Pouch)
Duavee 0.45 mg/20 mg conjugated estrogens/bazedoxifene tablets film coated oral medication by U.S. Pharmaceuticals. The package contains 7 tablets in 1 blister card. The label states this is a professional sample not for sale and includes usage instructions to use within 60 days after opening the foil pouch and to store in the original package to protect from moisture.*
FDA Label Image

Principal Display Panel (7 Tablet Carton)

Principal Display Panel (7 Tablet Carton)
Duavee 0.45 mg/20 mg tablets packaging label showing the product name, dosage strength, and active ingredients conjugated estrogens and bazedoxifene. The label indicates 7 film-coated tablets in a blister card, with storage instructions and a note that the product is a professional sample not for sale. The labeler is U.S. Pharmaceuticals, and the package includes the Pfizer logo.*

* 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.