Dantrolene Injection, Powder, For Solution
Product Images NDC 0143-9297

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Dantrolene (NDC 0143-9297). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Hikma Pharmaceuticals Usa 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

Structure (Dantrolene Sodium For Injection Usp 1)

Chemical structure of dantrolene, showing its molecular arrangement including a nitrophenyl group, furan ring, hydrazone linkage, and a sodium salt of a hydantoin derivative with hydration.*

FDA Label Image

Container Label (Dantrolene Sodium For Injection Usp 2)

Dantrolene Sodium for Injection, USP powder for solution, labeled as 20 mg per vial. The label states it is for intravenous use only and a single dose vial. It includes storage instructions and preparatory information. Manufactured by Hikma Pharmaceuticals USA Inc., with NDC 0143-9297-01.*

FDA Label Image

Dantrolene Sodium For Injection Usp 3

Packaging label for Dantrolene Sodium for Injection, USP 20 mg per vial by Hikma Pharmaceuticals USA Inc. The carton is for a single-dose 20 mg vial intended for intravenous use only. The label indicates it is Rx only and states it is for treatment of malignant hyperthermia. Includes storage instructions and manufacturer information. The design features red, blue, and white colors with barcodes on the flaps.*

FDA Label Image

Dantrolene Sodium For Injection Usp 4

Label for Dantrolene injection powder for solution 20 mg/1 vial from Hikma Pharmaceuticals USA Inc. The label includes a QR code and printed information for GTIN, serial number, expiration date, and lot number.*

* 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.