Sodium Diuril
Product Images NDC 76478-711

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 Sodium Diuril (NDC 76478-711). 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

Sod07 0009 01

Sod07 0009 01
Chemical structure of Sodium Diuril, showing its molecular arrangement including sulfonamide, chlorine, and sodium components as part of the active ingredient's formula.*
FDA Label Image

Sod07 0009 02

Sod07 0009 02
Chemical structure diagram of the active ingredient for Sodium Diuril by Akorn. The structure shows a chlorinated benzene ring with a sulfonamide group and a heterocyclic ring including nitrogen and sulfur atoms.*
FDA Label Image

Sod07 0009 03

Sod07 0009 03
The image shows a label for Sodium Diuril (chlorothiazide sodium) 0.5 g in a single dose vial for intravenous use. The label states the product is for the preparation of intravenous solutions, contains directions for dosage and storage, and is distributed by Akorn Operating Company LLC. The label includes the NDC 76478-711-40 and a barcode.*
FDA Label Image

Sod07 0009 04

Sod07 0009 04
Packaging label for Sodium Diuril 0.5 g intravenous single dose vial by Akorn. The label highlights chlorothiazide sodium as the active ingredient, with dosing and preparation instructions for intravenous solutions. It includes storage conditions, inactive ingredients, and distributor information for Akorn Operating Company LLC.*

* 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.