Chlorothiazide Injection, Powder, Lyophilized, For Solution
Product Images NDC 63323-658

5 FDA label images from Fresenius Kabi Usa, Llc · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 5 technical images submitted to the FDA as part of the official labeling for Chlorothiazide (NDC 63323-658). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Fresenius Kabi Usa, Llc, 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

Vial (402807a)

Vial (402807a)
Chlorothiazide Sodium injection powder, lyophilized, for solution, USP 500 mg per vial. The label indicates it is for intravenous use only, single-dose vial, prescription drug. The product is labeled by Fresenius Kabi USA, LLC under the PremierProRx brand.*
FDA Label Image

Pbox (621292a)

Pbox (621292a)
Label for Chlorothiazide Sodium injection, USP, 500 mg per vial. The label indicates it is for preparation of intravenous solutions, prescription only, and a single-dose vial. The labeler is Premier ProRx.*
FDA Label Image
FDA Label Image

Chlor Structure1

Chlor Structure1
Chemical structure of Chlorothiazide sodium, showing its molecular arrangement including a benzothiadiazine ring with chlorine, sulfonamide, and sodium groups.*
FDA Label Image

Chlor Structure2

Chlor Structure2
Chemical structure of chlorothiazide sodium showing a benzothiazide core with substituents including chlorine, sulfonamide, and other functional groups, consistent with the active ingredient in the chlorothiazide injection powder product.*

* 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.