Chlorothiazide Sodium
Product Images NDC 17478-419

4 FDA label images from Akorn · 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 Chlorothiazide Sodium (NDC 17478-419). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Akorn, these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.

Product Images & Figures Index

FDA Label Image

Chl02 0005 01

Chl02 0005 01
Chemical structure of Chlorothiazide Sodium showing a benzothiadiazine ring with chlorine, sulfonamide, sodium, and other substituents as part of the molecule.*
FDA Label Image

Chl02 0005 02

Chl02 0005 02
Chemical structure of Chlorothiazide Sodium showing a benzothiadiazine ring with chlorine, sulfonamide, and sulfone functional groups.*
FDA Label Image

Chl02 0005 03

Chl02 0005 03
Label for Chlorothiazide Sodium for Injection, USP, 500 mg per vial, sterile and lyophilized, distributed by Akorn, Inc. The label states the vial is for preparation of intravenous solutions and is single-dose. It includes instructions to reconstitute with 18 mL sterile water and dosing guidance for adults. Active ingredient strength and storage conditions are noted, along with an NDC and barcode.*
FDA Label Image

Chl02 0005 04

Chl02 0005 04
Packaging label for Chlorothiazide Sodium for Injection, USP, 500 mg per vial, sterile lyophilized powder, distributed by Akorn. The label includes instructions for reconstitution with sterile water for injection, specifies single-dose vial usage, and highlights the product is for preparation of intravenous solutions. Storage instructions and inactive ingredients are also provided.*

* 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.