Danazol Capsule
Product Images NDC 0555-0633

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 0555-0633). 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

FDA Label Image

Image 2

Image 2
Danazol is a medication that comes in the form of 50mg capsules. The NDC number is 0555-0633-02 and the GTIN number is 0030550633020. The revision date of the package is 10/2015, and the letter B indicates that it is only available through prescription. There is additional text that cannot be accurately interpreted.*
FDA Label Image

Image 3

Image 3
This is a description of a medication in capsule form with a strength of 100mg per capsule. The National Drug Code (NDC) is 0555-0634-02 and the Global Trade Item Number (GTIN) is 0030550634027. The medication should be stored at a temperature ranging from 68° to 77°F (25°C). The label contains a warning to keep the medication out of reach of children. The rest of the text is not readable.*
FDA Label Image

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Image 4
This text contains information about Danazol capsules of 200 mg with GTIN code 00305. The capsules come in a pack of 60 tablets marked as j only. The revision of this medication was done in October 2015. Customers are advised to keep this medication out of children's reach. There is also a lot number and expiry date present.*

* 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.