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Rizatriptan

Generic Name
Rizatriptan
Brand Names
Maxalt, Rizaport
Drug Type
Small Molecule
Chemical Formula
C15H19N5
CAS Number
144034-80-0
Unique Ingredient Identifier
51086HBW8G

Overview

Rizatriptan is a second-generation triptan and a selective 5-HT receptor agonist. Used in the treatment of migraines, rizatriptan was first approved in the US in 1998. Rizatriptan is available in oral tablets, orally disintegrating tablets (wafers), and oral film formulations.

Background

Rizatriptan is a second-generation triptan and a selective 5-HT receptor agonist. Used in the treatment of migraines, rizatriptan was first approved in the US in 1998. Rizatriptan is available in oral tablets, orally disintegrating tablets (wafers), and oral film formulations.

Indication

Rizatriptan is indicated for the acute treatment of diagnosed migraine with or without aura. Rizatriptan is not indicated for the prophylactic therapy of migraine nor the treatment of cluster headache. In Canada, rizatriptan is approved in adults. In the US, the oral tablet formulations are used in patients six years of age and older and the oral film formation is approved for patients 12 years of age and older weighing 40 kg or more.

Associated Conditions

  • Migraine With Aura
  • Migraine Without Aura
  • Migraine with acute onset aura

Clinical Trials

Phase 3
Completed
Posted: 2020/05/12
Sponsor:
Eurofarma Laboratori...
Phase 2
Completed
Posted: 2015/05/19
Sponsor:
Robert W. Baloh

FDA Approved Products

rizatriptan benzoate
Manufacturer:A-S Medication Solutions
Route:ORAL
Strength:10 mg in 1 1
Approved: 2021/02/18
NDC:50090-4619
RIZATRIPTAN BENZOATE
Manufacturer:direct rx
Route:ORAL
Strength:10 mg in 1 1
Approved: 2023/05/04
NDC:72189-258
rizatriptan benzoate
Manufacturer:Jubilant Cadista Pharmaceuticals Inc.
Route:ORAL
Strength:10 mg in 1 1
Approved: 2021/02/18
NDC:59746-415
Rizatriptan Benzoate
Manufacturer:NuCare Pharmaceuticals,Inc.
Route:ORAL
Strength:10 mg in 1 1
Approved: 2024/02/02
NDC:68071-3568
Rizatriptan Benzoate
Manufacturer:Aurobindo Pharma Limited
Route:ORAL
Strength:5 mg in 1 1
Approved: 2024/02/17
NDC:65862-599

Singapore Approved Products

No Singapore products found for this drug

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