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Tradename: MAXALT-MLT
Summary for Tradename: MAXALT-MLT
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Clinical Trials for: MAXALT-MLTLong-Term Exposure to Rizatriptan 5-mg and 10-mg Oral Tablet (Combined Extension Protocols MK-0462-022, MK-0462-025, MK-0462-029) Status: Completed Condition: Migraine Disorders Drug Study in Pediatric Subjects With Migraines (MK0462-083 AM1) Status: Completed Condition: Migraine Disorders Rizatriptan 5 mg and 10 mg, Sumatriptan 100 mg, and Placebo Comparison Study (0462-030)(COMPLETED) Status: Completed Condition: Migraine Headache A Study to Evaluate the Efficacy and Tolerability of Rizatriptan for Treatment of Acute Migraine in Children and Adolescents (MK-0462-082 AM7) Status: Completed Condition: Migraine, Acute Study of Rizatriptan in the Treatment of Acute Attacks of Post-traumatic Headache in U.S. Military Troops Status: Recruiting Condition: Chronic Post-traumatic Headache MK0462 in Treatment of Migraine With Recurrence (MK0462-022)(COMPLETED) Status: Completed Condition: Migraine Headache Two Rizatriptan Prescribing Portions for Treatment of Migraine Status: Completed Condition: Migraine A Study to Evaluate the Safety and Tolerability of Rizatriptan for Long Term Treatment of Acute Migraine in Children and Adolescents (MK-0462-086 AM3) Status: Completed Condition: Acute Migraine With or Without Aura in Adolescents Maxalt 10mg Plus Caffeine 75mg in the Acute Treatment of Migraine Headache Status: Completed Condition: Migraine With Aura; Migraine Without Aura MK0462 5 mg, Sumatriptan 50 mg, and Placebo Comparison Study (0462-029)(COMPLETED) Status: Completed Condition: Migraine Headache Courtesy of ClinicalTrials.org See more clinical trials for this drug | ||||||||||||
Glossary
| Applicant | Tradename | Generic Name | Dosage | NDA | Approval Date | Type | RLD | Patent No. | Product | Substance | Delist_Flag | Patent Expiration | Exclusivity Expiration | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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Merck | MAXALT-MLT | rizatriptan benzoate | TABLET, ORALLY DISINTEGRATING; ORAL | 020865 | Jun 29, 1998 | RX | No | <disabled> | <disabled> | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Merck | MAXALT-MLT | rizatriptan benzoate | TABLET, ORALLY DISINTEGRATING; ORAL | 020865 | Jun 29, 1998 | RX | No | <disabled> | <disabled> | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Merck | MAXALT-MLT | rizatriptan benzoate | TABLET, ORALLY DISINTEGRATING; ORAL | 020865 | Jun 29, 1998 | RX | No | 5,298,520*PED | <disabled> | <disabled> | |||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Merck | MAXALT-MLT | rizatriptan benzoate | TABLET, ORALLY DISINTEGRATING; ORAL | 020865 | Jun 29, 1998 | RX | No | 5,457,895*PED | Y | <disabled> | <disabled> | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
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Paragraph IV activity for: MAXALT-MLT
| Drugname | Dosage | Strength | RLD | Submissiondate |
| rizatriptan benzoate | Orally Disintegrating Tablets | 5 mg and 10 mg | Maxalt-MLT | 2/17/2006 |
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