Succinylcholine Chloride Injection, Solution
Product Images NDC 71872-7167

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Succinylcholine Chloride (NDC 71872-7167). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Medical Purchasing Solutions, 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

71872-7167-1 (71872 7167 1)

Succinylcholine Chloride Injection is a paralyzing agent used for intravenous or intramuscular use. It comes in a single vial with a quantity of 10 ml and a strength of 200 mg per 10 ml. The drug contains succinylcholine chloride, methylparaben, and propylparaben as preservatives. The vial should be used only if the seal is intact and undamaged. A warning is given that the drug may cause respiratory arrest, and facilities for artificial respiration should be available. The product should be stored in a refrigerator between 2°C to 8°C. The name of the manufacturer is Ronaissance Pharmaceuticals Inc., Lakewood, NJ 08701, and it is manufactured for Amring Pharmaceuticals Inc., Bervyn, PA 19312.*

FDA Label Image

1 (Succinylcholine Structure)

FDA Label Image

Company (Succinylcholine Company)

FDA Label Image

Vial Label (Succinylcholine Label)

This is a prescription-only drug containing 0.18% methylparaben and 0.02% propylparaben as preservatives. It is sterile and nonpyrogenic, and should be stored at 2° to 8°C. The drug is Chloride Injection, USP, and is manufactured by Renaissance Pharmaceuticals Inc. It should be used with caution, as it is a paralyzing agent for intravenous or intramuscular use. This drug is intended to be used by professionals who are trained in its administration.*

* 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.