Danazol Capsule
Product Images NDC 71205-862

3 FDA label images from Proficient Rx Lp · 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 Danazol (NDC 71205-862). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Proficient Rx Lp, 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

Danazol Molecular Structure (Danazol Capsules Usp 50 mg 100 mg And 200 mg 1)

Danazol Molecular Structure (Danazol Capsules Usp 50 mg 100 mg And 200 mg 1)
Chemical structure of the active ingredient Danazol. The structure shows the molecular arrangement including multiple rings, methyl groups, a hydroxyl group, and a nitrile moiety.*
FDA Label Image

71205-861-30 (Danazol Capsules Usp 50 mg 100 mg And 200 mg 3)

71205-861-30 (Danazol Capsules Usp 50 mg 100 mg And 200 mg 3)
Danazol 100 mg capsules label by Proficient Rx LP. The label indicates a 30-count package of oral capsules, each containing 100 mg of Danazol. Capsules are maize opaque with the imprint "LANNETT" on the cap and "1368" on the body. Distributed by Lannett Company, Philadelphia, PA.*
FDA Label Image

71205-862-30 (Danazol Capsules Usp 50 mg 100 mg And 200 mg 4)

71205-862-30 (Danazol Capsules Usp 50 mg 100 mg And 200 mg 4)
Danazol 200 mg capsules label by Proficient Rx LP. The label indicates a quantity of 30 capsules, each containing 200 mg of Danazol, USP. Capsules are described as orange opaque with specific imprints: "LANNETT" on the cap and "1369" on the body. The label includes storage instructions and distributor information for Lannett Company, Inc.*

* 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.