Succinylcholine Chloride Injection, Solution
Product Images NDC 70069-301

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Succinylcholine Chloride (NDC 70069-301). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Somerset Therapeutics, 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

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Chemical structure of succinylcholine chloride showing two quaternary ammonium groups, ester linkages, and chloride ions. The structural diagram represents the molecular arrangement of the active ingredient succinylcholine chloride.*

FDA Label Image

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Label for Succinylcholine Chloride Injection, USP 20 mg/mL (200 mg/10 mL) solution for injection. The label indicates it is a 10 mL multiple dose vial for intravenous or intramuscular use. It includes warnings about its paralyzing effect and storage instructions, and lists Somerset Therapeutics, LLC as the manufacturer.*

FDA Label Image

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Label for Succinylcholine Chloride Injection, USP 20 mg/mL by Somerset Therapeutics LLC. The label indicates a 200 mg/10 mL concentration in multiple dose vials (10 x 10 mL). It states use for intravenous or intramuscular injection with refrigeration storage instructions, warnings about paralysis and respiratory arrest, and manufacturing details including origin in India.*

FDA Label Image

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Label for Succinylcholine Chloride Injection, USP 200 mg/10 mL (20 mg/mL) solution for injection by intravenous or intramuscular use. The label states the product is a paralyzing agent and includes storage instructions to keep refrigerated at 2°-8°C (36°-46°F). It is manufactured for Somerset Therapeutics, LLC and is packaged as 25 multiple dose vials of 10 mL each.*

* 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.