Danazol Capsule
Product Images NDC 0555-0634

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Danazol (NDC 0555-0634). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Teva Pharmaceuticals 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

Image 1

Image 1
Chemical structure diagram of the active ingredient Danazol. The structure shows the molecular framework with rings, functional groups, and chemical bonds typical for Danazol.*
FDA Label Image

Image 2

Image 2
Label for Danazol Capsules USP 50 mg by Teva Pharmaceuticals USA, Inc. The label includes dosage information stating each capsule contains 50 mg danazol. It specifies usual dosage and storage instructions at 20° to 25°C, with light-resistant container requirements. The label also notes this product is prescription only and contains 100 capsules per container.*
FDA Label Image

Image 3

Image 3
Label for Danazol Capsules USP 100 mg by Teva Pharmaceuticals USA, Inc. The label indicates a package containing 100 capsules. It provides storage instructions at 20° to 25°C and includes standard warnings about dispensing and prescription use. The NDC number 0555-0634-02 is visible.*
FDA Label Image

Image 4

Image 4
Danazol Capsules USP 200 mg oral capsules label by Teva Pharmaceuticals USA, Inc. The label shows the product name, strength, NDC 0555-0635-09, a 60-capsule package size, and storage instructions. It includes dosage and safety information placeholders and a barcode.*

* 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.