Succinylcholine Chloride
Product Images NDC 51662-1353

5 FDA label images from Hf Acquisition Co Llc, Dba Healthfirst · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 5 technical images submitted to the FDA as part of the official labeling for Succinylcholine Chloride (NDC 51662-1353). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Hf Acquisition Co Llc, Dba Healthfirst, 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

How Supplied (How Supplied)

How Supplied (How Supplied)
Data table showing NDC numbers, container types, sizes, concentrations (mg/mL), total milligrams, and calculated mOsmol/mL for single-dose and multiple-dose fliptops vials of Succinylcholine Chloride.*
FDA Label Image
FDA Label Image

Serialized Label (Serialized Label)

Serialized Label (Serialized Label)
A clear glass vial of SUCCINYLCHOLINE CHLORIDE injection labeled with an orange and white label indicating a strength of 200 mg (20 mg/mL) and a 10 mL volume. The vial has a red cap with white text warning it is a paralyzing agent. The labeler is HF Acquisition Co LLC, DBA HealthFirst. A barcode and additional product information appear on a white sticker affixed to the side.*
FDA Label Image

Structure (Structure Description)

Structure (Structure   Description)
Chemical structure of Succinylcholine Chloride showing two quaternary ammonium groups and associated chloride ions.*
FDA Label Image

Vial Label Updated (Vial Label Updated)

Vial Label Updated (Vial Label Updated)
Label for SUCCINYLCHOLINE CHLORIDE Injection USP 200 mg/10 mL (20 mg/mL) by HF Acquisition Co LLC, DBA HealthFirst. The 10 mL vial label includes warnings stating it is a paralyzing agent causing respiratory arrest, indicating the need for facilities equipped for artificial respiration. Storage instructions specify 2° to 8°C. The label also notes preservatives and distribution by Hospira, Inc.*

* 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.