Succinylcholine Chloride Injection, Solution
Product Images NDC 65219-276

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 9 technical images submitted to the FDA as part of the official labeling for Succinylcholine Chloride (NDC 65219-276). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Fresenius Kabi Usa 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

Figure (Suc0a 0004 01)

Figure (Suc0a 0004 01)
An instructional labeled diagram depicting a prefilled syringe of Succinylcholine Chloride injection, solution 20 mg/mL. The image shows the syringe in outer package (flow wrap) on the left and the syringe components on the right, including the plunger rod, syringe barrel with label, and syringe tip cap.*
FDA Label Image

Figure (Suc0a 0004 02)

Figure (Suc0a 0004 02)
An instructional line drawing showing two hands preparing a syringe by removing it from sterile packaging, illustrating aseptic technique for injection preparation.*
FDA Label Image

Figure (Suc0a 0004 03)

Figure (Suc0a 0004 03)
An instructional diagram showing hands removing or attaching a small component to the end of a syringe barrel by twisting and pulling motions, indicated by arrows. The illustration focuses on syringe assembly or disassembly technique, relevant to preparation or use of an injectable solution.*
FDA Label Image

Figure (Suc0a 0004 04)

Figure (Suc0a 0004 04)
Chemical structure of Succinylcholine Chloride shown as a molecular diagram including two quaternary ammonium groups and associated chloride ions, with hydration indicated by two water molecules (2H2O).*
FDA Label Image

Fresenius Kabi Logo (Suc0a 0004 05)

FDA Label Image

Package Label (PRINCIPAL DISPLAY – Succinylcholine 10 mL Sticker Label)

Package Label (PRINCIPAL DISPLAY – Succinylcholine 10 mL Sticker Label)
Label for Succinylcholine Chloride Injection, USP Special Solution. The label includes repeated warning text indicating it is a paralyzing agent causing respiratory arrest and requiring facilities for artificial respiration. It has fields for concentration (mg/mL), date, name of basic solution used, and operating suite or other use location. The labeler is Fresenius Kabi USA LLC, consistent with the product.*
FDA Label Image

Package Label (PRINCIPAL DISPLAY – Succinylcholine 10 mL RFID Syringe Label)

Package Label (PRINCIPAL DISPLAY – Succinylcholine 10 mL RFID Syringe Label)
Label for Succinylcholine Chloride Injection, USP 200 mg/10 mL (20 mg/mL) solution in a 10 mL single-dose prefilled syringe. The label includes warnings about respiratory arrest, dosage form, storage instructions at 2°C to 8°C, and manufacturer Fresenius Kabi USA LLC. The product is preservative-free and intended for intravenous or intramuscular administration.*
FDA Label Image

Package Label (PRINCIPAL DISPLAY – Succinylcholine 10 mL RFID Shipper Label)

Package Label (PRINCIPAL DISPLAY – Succinylcholine 10 mL RFID Shipper Label)
Label for Succinylcholine Chloride Injection, USP, 200 mg/10 mL (20 mg/mL) solution for injection. The label includes warnings about respiratory arrest and use only for intravenous or intramuscular administration. The product is preservative-free and supplied in 10 x 10 mL single-dose prefilled syringes. Manufactured for Fresenius Kabi USA LLC, with storage instructions at 2°C to 8°C (36°F to 46°F).*
FDA Label Image

Package Label (PRINCIPAL DISPLAY – Succinylcholine 10 mL RFID Shipper Label)

Package Label (PRINCIPAL DISPLAY – Succinylcholine 10 mL RFID Shipper Label)
Label for Succinylcholine Chloride Injection USP 200 mg/10 mL (20 mg/mL) manufactured by Fresenius Kabi USA LLC. The label indicates packaging of 16 packs of 10 syringes (160 syringes total), with storage instructions to keep refrigerated at 2°C to 8°C (36°F to 46°F). The product is made in Austria and includes the NDC 65219-276-10.*

* 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.