MedPath

Citicoline

Generic Name
Citicoline
Drug Type
Small Molecule
Chemical Formula
C14H26N4O11P2
CAS Number
987-78-0
Unique Ingredient Identifier
536BQ2JVC7

Overview

Citicoline is a donor of choline in biosynthesis of choline-containing phosphoglycerides. It has been investigated for the treatment, supportive care, and diagnosis of Mania, Stroke, Hypomania, Cocaine Abuse, and Bipolar Disorder, among others.

Indication

主要用于急性颅脑外伤和脑手术后的意识障碍,以及脑卒中而致偏瘫的患者;也用于耳鸣及神经性耳聋、急性中毒、感染、大面积脑梗死所致的昏迷和意识障碍、帕金森病、急性胰腺炎;对缺血性脑血管病和血管性痴呆也有一定疗效,但对颅内出血引起的意识障碍效果较差。

Associated Conditions

  • Degenerative Brain Disorder
  • Parkinsonian Syndromes

FDA Drug Approvals

Approved Product
Manufacturer
NDC Code
Route
Strength
Effective Date
No FDA approvals found for this drug.

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
No HSA approvals found for this drug.

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
SOMAZINA ORAL SOLUTION 100MG/ML
N/A
N/A
N/A
5/10/2017
SOMAZINA ORAL SOLUTION 1000MG IN 10ML SACHET
N/A
N/A
N/A
12/1/2021

TGA Drug Approvals

Approved Product
ARTG ID
Sponsor
Registration Type
Status
Registration Date
No TGA 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
SOMAZINA 500 mg SOLUCION INYECTABLE
54390
SOLUCIÓN INYECTABLE
Medicamento Sujeto A Prescripción Médica
Commercialized
SOMAZINA 1g SOLUCION INYECTABLE
54389
SOLUCIÓN INYECTABLE
Medicamento Sujeto A Prescripción Médica
Commercialized
SOMAZINA 100 mg/ml SOLUCION ORAL
53168
SOLUCIÓN ORAL
Medicamento Sujeto A Prescripción Médica
Commercialized

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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