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Succinylcholine

Generic Name
Succinylcholine
Brand Names
Anectine, Quelicin
Drug Type
Small Molecule
Chemical Formula
C14H30N2O4
CAS Number
306-40-1
Unique Ingredient Identifier
J2R869A8YF

Overview

Succinylcholine is a depolarizing skeletal muscle relaxant consisting of two molecules of the endogenous neurotransmitter acetylcholine (ACh) linked by their acetyl groups. It has been widely used for over 50 years, most commonly in its chloride salt form, as a means of neuromuscular blockade during intubation and surgical procedures. Its rapid onset and offset, with effects beginning within 60 seconds of intravenous administration and lasting between four to six minutes, make succinylcholine particularly useful in the setting of short medical procedures requiring brief periods of muscle relaxation.

Indication

Succinylcholine is indicated as an adjunct to general anesthesia, to facilitate tracheal intubation, and to provide skeletal muscle relaxation during surgery or mechanical ventilation.

Associated Conditions

No associated conditions information available.

Clinical Trials

Title
Posted
Study ID
Phase
Status
Sponsor
2024/11/29
Not Applicable
Not yet recruiting
Peng Liang
2023/09/08
Phase 4
Recruiting
2022/09/27
Phase 4
Completed
China-Japan Friendship Hospital
2021/05/03
Phase 4
Completed
Matias Vested
2020/10/09
Phase 3
Completed
2018/05/22
Phase 2
Completed
2018/03/19
Not Applicable
UNKNOWN
2016/09/26
N/A
Completed
Jakob Louis Thomsen
2016/07/04
Phase 3
Completed
Rennes University Hospital
2016/02/05
Phase 2
Completed

FDA Drug Approvals

Approved Product
Manufacturer
NDC Code
Route
Strength
Effective Date
Hikma Pharmaceuticals USA Inc.
0143-9338
INTRAMUSCULAR, INTRAVENOUS
20 mg in 1 mL
6/26/2023
Hikma Pharmaceuticals USA Inc.
0641-6234
INTRAMUSCULAR, INTRAVENOUS
20 mg in 1 mL
1/2/2024

EMA Drug Approvals

Approved Product
Authorization Holder
Status
Issued Date
No EMA approvals found for this drug.

HSA Drug Approvals

Approved Product
Manufacturer
Approval Number
Dosage Form
Strength
Approval Date
ETHICHOLINE INJECTION 100 mg/2 ml
SIN05861P
INJECTION
103 mg/2mL
5/13/1991
MARTINDALE PHARMA SUXAMETHONIUM CHLORIDE SOLUTION FOR INJECTION 50MG/ML
SIN15643P
INJECTION, SOLUTION
50MG/ML
3/8/2019

NMPA Drug Approvals

Approved Product
Company
Approval Number
Drug Type
Dosage Form
Approval Date
No NMPA approvals found for this drug.

PPB Drug Approvals

Approved Product
Registration No.
Company
Licence No.
Strength
Registration Date
No PPB approvals found for this drug.

Health Canada Drug Approvals

Approved Product
Company
DIN
Dosage Form
Strength
Market Date
No Health Canada approvals found for this drug.

CIMA AEMPS Drug Approvals

Approved Product
Company
Registration Number
Pharmaceutical Form
Prescription Type
Status
No CIMA AEMPS (Spain) approvals found for this drug.

Philippines FDA Drug Approvals

Approved Product
Company
License Number
Dosage Form
Strength
Approval Date
No Philippines FDA approvals found for this drug.

Saudi SFDA Drug Approvals

Approved Product
Company
License Number
Dosage Form
Strength
Approval Date
No Saudi SFDA approvals found for this drug.

Malaysia NPRA Drug Approvals

Approved Product
Company
Registration Number
Dosage Form
Strength
Approval Date
No Malaysia NPRA approvals found for this drug.

UK EMC Drug Information

Medicine Name
MA Holder
MA Number
Pharmaceutical Form
Active Ingredient
Authorization Date
No UK EMC drug information found for this drug.

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