MedPath

Vardenafil

Generic Name
Vardenafil
Brand Names
Levitra, Staxyn
Drug Type
Small Molecule
Chemical Formula
C23H32N6O4S
CAS Number
224785-90-4
Unique Ingredient Identifier
UCE6F4125H

Overview

Vardenafil is a selective inhibitor of cyclic guanosine monophosphate (cGMP)-specific phosphodiesterase type 5 (PDE5) and an oral therapy for the treatment of erectile dysfunction. During sexual stimulation, nitric oxide (NO) is released from nerve endings and endothelial cells in the corpus cavernosum, activating the enzyme guanylate cyclase and increasing the synthesis of cGMP in the smooth muscle cells of the corpus cavernosum. PDE5 inhibitors, such as vardenafil, inhibit the degradation of cGMP and allow increased blood flow into the penis, resulting in an erection.. Compared to sildenafil and tadalafil, vardenafil is a more potent inhibitor of PDE5; however, its selectivity for other PDE isoforms is lower than the one detected for tadalafil. The FDA approved the use of vardenafil for the treatment of erectile dysfunction in 2003. Although other PDE5 inhibitors such as sildenafil and tadalafil have been associated with rare cases of acute liver injury, the use of vardenafil has not been linked to hepatotoxic effects. The use of vardenafil as a monotherapy for the treatment of pulmonary arterial hypertension has also been evaluated.

Indication

Vardenafil is indicated for the treatment of erectile dysfunction.

Associated Conditions

  • Erectile Dysfunction

Clinical Trials

Title
Posted
Study ID
Phase
Status
Sponsor
2025/03/06
Phase 1
Completed
2024/07/08
Phase 3
Recruiting
2022/10/05
Phase 1
Completed
2017/04/05
Phase 1
UNKNOWN
2015/05/21
Phase 4
Completed
2015/01/26
Phase 4
UNKNOWN
2014/10/31
Early Phase 1
Terminated
2014/08/19
Phase 2
Completed
Azienda USL Modena
2012/07/25
Phase 4
UNKNOWN
2011/08/01
N/A
TEMPORARILY_NOT_AVAILABLE

FDA Drug Approvals

Approved Product
Manufacturer
NDC Code
Route
Strength
Effective Date
QYK BRANDS LLC
73750-104
ORAL
10 mg in 1 1
3/31/2022
Macleods Pharmaceuticals Limited
33342-203
ORAL
11.85 mg in 1 1
9/30/2023
Zydus Pharmaceuticals USA Inc.
70710-1068
ORAL
2.5 mg in 1 1
5/30/2023
Zydus Lifesciences Limited
70771-1048
ORAL
5 mg in 1 1
10/31/2022
Macleods Pharmaceuticals Limited
33342-154
ORAL
20 mg in 1 1
4/10/2023
Macleods Pharmaceuticals Limited
33342-151
ORAL
2.5 mg in 1 1
4/10/2023
Macleods Pharmaceuticals Limited
33342-153
ORAL
10 mg in 1 1
4/10/2023
QYK BRANDS LLC
73750-102
ORAL
2.5 mg in 1 1
3/31/2022
QYK BRANDS LLC
73750-103
ORAL
5 mg in 1 1
3/31/2022
Alembic Pharmaceuticals Inc.
62332-235
ORAL
10 mg in 1 1
9/15/2023

EMA Drug Approvals

Approved Product
Authorization Holder
Status
Issued Date
Authorised
3/6/2003

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
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
LEVITRA 20mg comprimidos recubiertos con pelicula
03248010IP4
COMPRIMIDO RECUBIERTO CON PELÍCULA
Medicamento Sujeto A Prescripción Médica
Not 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.

Help Us Improve

Your feedback helps us provide better drug information and insights.

MedPath

Empowering clinical research with data-driven insights and AI-powered tools.

© 2025 MedPath, Inc. All rights reserved.