Sodium-diuril-01 (Chlorothiazide Sodium For Injection Usp 1)
Chlorothiazide Sodium Injection, Powder, Lyophilized, For Solution
Product Images NDC 0517-1820
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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.
Sodium-diuril-02 (Chlorothiazide Sodium For Injection Usp 2)
Container (Chlorothiazide Sodium For Injection Usp 3)
This is a description of Chlorothiazide Sodium for injection. It is used as a medication to help eliminate excess water and salt from the body. It comes in the form of a single, sterile, freeze-dried vial that contains 500 mg of Chlorothiazide Sodium, along with Mannitol and Sodium Fycronde. The medication should be reconstituted with a minimum of 18 ml of sterile water for injection. The reconstituted solution should be used immediately as a single dose. Unused portions should be discarded. The medication should be stored at temperatures between 20°C and 25°C. The usual adult dosage should be determined by a healthcare professional.*
Carton (Chlorothiazide Sodium For Injection Usp 4)
Chlorothiazide Sodium For Injection Usp 5
This appears to be a product testing label with a LOT number, an expiration date of November 2020, a GTIN (Global Trade Item Number) of 00305171820014, and an SN (serial number) of 0. Without additional context, it is not possible to determine the specific product being tested.*
* 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.
