MedPath

Vasopressin

Generic Name
Vasopressin
Brand Names
Vasostrict
Drug Type
Small Molecule
Chemical Formula
C92H130N28O24S4
CAS Number
11000-17-2
Unique Ingredient Identifier
Y87Y826H08

Overview

Vasopressin (arginine-vasopressin or antidiuretic hormone) is a nonapeptide primarily produced in the hypothalamus that exhibits diverse physiological functions related to diuresis, hemodynamic modulation, and behaviour. Vasopressin is very similar to oxytocin, differing in the third and eighth amino acids. Despite a wide variety of functions, exogenous vasopressin is primarily used to control blood pressure during systemic shock by increasing vasoconstriction and renal fluid reuptake by acting through V and V cellular receptors. The vasopressive effect of posterior pituitary gland extracts was noted in 1895, while vasopressin itself was not purified until 1951. It has been used for more than five decades for varying conditions, including variceal bleeding, diabetes insipidus, and, more recently, vasodilatory shock. It is currently marketed under the trademark VASOSTRICT® by PAR Pharmaceuticals.

Indication

1.诊断和治疗由于缺乏抗利尿激素而引起的尿崩症,也用于其他药物效果不佳的腹部肌肉松弛; 2.脑外科手术后或头颅创伤后多尿的初期治疗; 3.用于食管、胃肠道消化道疾病的急性大出血的辅助治疗。

Associated Conditions

  • Acute Circulatory Failure

Clinical Trials

Title
Posted
Study ID
Phase
Status
Sponsor
2024/11/29
Phase 4
Recruiting
2024/09/20
Not Applicable
ENROLLING_BY_INVITATION
University of Electronic Science and Technology of China
2024/08/09
Phase 2
Recruiting
2024/06/24
Phase 4
Recruiting
2024/06/18
Phase 3
Recruiting
2024/05/23
N/A
Not yet recruiting
2024/05/21
N/A
Recruiting
Hospital Universitario 12 de Octubre
2024/05/17
Phase 4
Withdrawn
2024/03/25
Not Applicable
Recruiting
University of Electronic Science and Technology of China
2024/03/25
Not Applicable
Recruiting
University of Electronic Science and Technology of China

FDA Drug Approvals

Approved Product
Manufacturer
NDC Code
Route
Strength
Effective Date
Medical Purchasing Solutions, LLC
71872-7306
INTRAVENOUS
20 [USP'U] in 1 mL
11/2/2023
Medical Purchasing Solutions, LLC
71872-7264
INTRAVENOUS
20 [USP'U] in 1 mL
5/3/2023
American Regent, Inc.
0517-1030
INTRAVENOUS
20 [USP'U] in 1 mL
1/1/2023
Eagle Pharmaceuticals, Inc.
42367-570
PARENTERAL
20 U in 1 mL
3/9/2023
American Regent, Inc.
0517-1020
INTRAVENOUS
20 [USP'U] in 1 mL
1/1/2023
Medical Purchasin Solutions, LLC
71872-7014
INTRAVENOUS
20 [USP'U] in 1 mL
6/1/2023
Par Pharmaceutical, Inc.
42023-220
INTRAVENOUS
0.6 [USP'U] in 1 mL
11/16/2023
Par Pharmaceutical, Inc.
42023-164
INTRAVENOUS
20 [USP'U] in 1 mL
11/16/2023
Gland Pharma Limited
68083-520
INTRAVENOUS
20 [USP'U] in 1 mL
2/14/2024
Fresenius Kabi USA, LLC
63323-930
INTRAVENOUS
20 [USP'U] in 1 mL
7/1/2022

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
VASOPRESSIN INJECTION USP 20 u/ml
SIN08350P
INJECTION
20 u/ml
9/19/1995

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.

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
VASOPRESSIN INJECTION, USP
fresenius kabi canada ltd
02139502
Solution - Subcutaneous ,  Intramuscular
20 UNIT / ML
8/14/1996
VASOPRESSIN INJ 20UNIT/ML USP
lyphomed, division of fujisawa canada inc.
01944800
Liquid - Subcutaneous ,  Intramuscular
20 UNIT / ML
12/31/1992
VASOPRESSIN INJ 20UNIT/ML USP
Ferring Inc
00693820
Liquid - Nasal ,  Intramuscular ,  Subcutaneous
20 UNIT / ML
12/31/1988
PITRESSIN INJ 10 UNIT/0.5ML
parke-davis division, warner-lambert canada inc.
00222577
Liquid - Subcutaneous ,  Intramuscular
10 UNIT / .5 ML
12/31/1971
VASOPRESSIN INJECTION USP
02247938
Solution - Intramuscular ,  Subcutaneous
20 UNIT / ML
12/10/2003

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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