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. |
TGA Drug Approvals
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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