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Eletriptan

Generic Name
Eletriptan
Brand Names
Relpax
Drug Type
Small Molecule
Chemical Formula
C22H26N2O2S
CAS Number
143322-58-1
Unique Ingredient Identifier
22QOO9B8KI

Overview

Eletriptan is a second generation triptan drug developed by Pfizer Inc for the treatment of migraine headaches.

Indication

For the acute treatment of migraine with or without aura in adults.

Associated Conditions

  • Migraine With Aura
  • Migraine Without Aura

Clinical Trials

Title
Posted
Study ID
Phase
Status
Sponsor
2024/11/06
Phase 1
Not yet recruiting
2013/11/21
Phase 3
Completed
Pfizer's Upjohn has merged with Mylan to form Viatris Inc.
2013/11/18
Phase 3
Completed
Pfizer's Upjohn has merged with Mylan to form Viatris Inc.
2013/11/18
Phase 3
Completed
Pfizer's Upjohn has merged with Mylan to form Viatris Inc.
2013/11/07
Phase 3
Completed
Pfizer's Upjohn has merged with Mylan to form Viatris Inc.
2013/05/22
Phase 3
Completed
Pfizer's Upjohn has merged with Mylan to form Viatris Inc.
2011/01/14
Not Applicable
Completed
California Medical Clinic for Headache
2010/06/08
Phase 1
Completed
Pfizer's Upjohn has merged with Mylan to form Viatris Inc.
2008/09/12
Phase 2
Completed
2008/03/13
Phase 4
Completed
Pfizer's Upjohn has merged with Mylan to form Viatris Inc.

FDA Drug Approvals

Approved Product
Manufacturer
NDC Code
Route
Strength
Effective Date
Ajanta Pharma USA Inc.
27241-040
ORAL
40 mg in 1 1
11/22/2021
Direct_Rx
72189-439
ORAL
40 mg in 1 1
3/27/2023
Ajanta Pharma USA Inc.
27241-039
ORAL
20 mg in 1 1
11/22/2021
Mylan Pharmaceuticals Inc.
0378-4287
ORAL
20 mg in 1 1
12/19/2018
ROERIG
0049-2330
ORAL
20 mg in 1 1
3/11/2020
Mylan Pharmaceuticals Inc.
0378-4288
ORAL
40 mg in 1 1
12/19/2018
Zydus Pharmaceuticals USA Inc.
68382-922
ORAL
20 mg in 1 1
9/18/2023
Teva Pharmaceuticals USA, Inc.
0093-8311
ORAL
40 mg in 1 1
7/25/2023
Amneal Pharmaceuticals LLC
65162-042
ORAL
20 mg in 1 1
8/19/2021
Amneal Pharmaceuticals LLC
65162-043
ORAL
40 mg in 1 1
8/19/2021

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
RELPAX TABLET 40 mg
SIN11767P
TABLET, FILM COATED
40 mg
1/14/2002

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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