Succinylcholine Chloride
Product Images NDC 52817-734

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Succinylcholine Chloride (NDC 52817-734). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Trupharma, 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

Principal Display Panel (20 mg/mL Carton)

Principal Display Panel (20 mg/mL Carton)
Succinylcholine Chloride Injection, USP 20 mg/10 mL (20 mg/mL) multiple-dose vials, labeled by Trupharma, LLC. The label states it is for intravenous or intramuscular use, with a paralyzing agent warning. Storage instructions specify refrigeration at 2° to 8°C. The box contains 25 vials of 10 mL each and includes additional usage and safety details.*
FDA Label Image

Structure (Structure)

Structure (Structure)
Chemical structure diagram of succinylcholine chloride, showing the molecular arrangement of its organic groups and chloride ions.*
FDA Label Image

Principal Display Panel (20 mg/mL Vial Label)

Principal Display Panel (20 mg/mL Vial Label)
Label for Succinylcholine Chloride Injection, USP, 200 mg/10 mL (20 mg/mL) by Trupharma, LLC. The label includes warnings for paralysis and respiratory arrest, instructions for intravenous or intramuscular use, preservative information, storage conditions, and manufacturer details. It indicates a 10 mL multiple-dose vial.*

* 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.