Chlorothiazide Sodium Injection, Powder, Lyophilized, For Solution
Product Images NDC 0517-1820

Product Visual Gallery

This gallery contains 5 technical images submitted to the FDA as part of the official labeling for Chlorothiazide Sodium (NDC 0517-1820). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by American Regent, 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

Sodium-diuril-01 (Chlorothiazide Sodium For Injection Usp 1)

Chemical structure diagram of Chlorothiazide Sodium, showing its molecular composition and arrangement with sodium, chlorine, nitrogen, sulfur, and oxygen atoms.*

FDA Label Image

Sodium-diuril-02 (Chlorothiazide Sodium For Injection Usp 2)

Chemical structure of Chlorothiazide Sodium, depicting its molecular composition with chlorine, sulfonamide, and heterocyclic components visible in the diagram.*

FDA Label Image

Container (Chlorothiazide Sodium For Injection Usp 3)

Chlorothiazide Sodium injection lyophilized powder label for intravenous use, 500 mg per vial, by American Regent, Inc. The label indicates it is a sterile single-dose vial intended for preparation of intravenous solutions. Storage instructions and formulation details are included, with a barcode on the right side.*

FDA Label Image

Carton (Chlorothiazide Sodium For Injection Usp 4)

Chlorothiazide Sodium 500 mg/vial lyophilized injection powder label for intravenous use by American Regent, Inc. The label includes preparation instructions for intravenous solutions, inactive ingredients, and storage conditions. The vial is for single-dose use only and is marked Rx Only.*

FDA Label Image

Chlorothiazide Sodium For Injection Usp 5

Label for Chlorothiazide Sodium injection powder, lyophilized, for solution, showing lot number 'TEST', expiration date November 2020, and GTIN barcode with number 00305171820014. The label does not display strength or manufacturer details but corresponds to the American Regent, Inc. product with NDC 0517-1820.*

* 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.