Succinylcholine Chloride Injection, Solution
Product Images NDC 69918-700

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Succinylcholine Chloride (NDC 69918-700). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Nordic Pharma, 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

Chemical Structure (Succinylcholine 01)

Chemical structure of suxamethonium chloride (succinylcholine chloride) with two chloride ions and two water molecules, showing molecular formula components and bonds.*

FDA Label Image

Carton 10 (Succinylcholine 12 Carton)

The label for Succinylcholine Chloride Injection, USP, 20 mg/mL strength by Nordic Pharma, Inc. It specifies a concentration of 200 mg/10 mL (20 mg/mL) in multiple-dose vials. The label warns that the product is a paralyzing agent causing respiratory arrest, indicating the need for facilities for artificial respiration. It notes storage in refrigerator at 2° to 8°C (36° to 46°F) and mentions sterile, nonpyrogenic use for intravenous or intramuscular administration. The label includes manufacturer details and batch information.*

FDA Label Image

Company (Succinylcholine Company)

FDA Label Image

Vial Label (Succinylcholine Label)

Label for Succinylcholine Chloride Injection, USP 20 mg/mL (200 mg/10 mL) multiple-dose vial by Nordic Pharma, Inc. It highlights storage instructions (2° to 8°C), preservative and excipient details, and a boxed warning about its paralyzing effects requiring immediate availability of artificial respiration. Manufactured by Biological E. Limited in India.*

* 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.