General MedicationsORALStandard
REYVOW
LASMIDITAN SUCCINATE
Standard Dose
EQ 100MG BASE
Max Dose
Refer to approved labeling
Primary Use
Review priority: STANDARD Marketing status: Prescription
Summary
Approval overview REYVOW is listed in Drugs@FDA under application 211280 (NDA).
Review priority: STANDARD Marketing status: Prescription Active ingredient LASMIDITAN SUCCINATE Form and strength TABLET;ORAL - EQ 100MG BASE Sponsor ELI LILLY AND CO Submission history Latest submission status date: 2022-09-15 00:00:00.
Structured Monograph
Clinical summary
Approval overview REYVOW is listed in Drugs@FDA under application 211280 (NDA). Review priority: STANDARD Marketing status: Prescription Active ingredient LASMIDITAN SUCCINATE Form and strength TABLET;ORAL - EQ 100MG BASE Sponsor ELI LILLY AND CO Submission history Latest submission status date: 2022-09-15 00:00:00. Submission type: SUPPL.
Monitoring
- • Marketing status: Prescription
- • Review priority: STANDARD
Interaction Notes
- No interaction notes stored yet.