REYVOW- lasmiditan tablet 
Eli Lilly and Company

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REYVOW (lasmiditan) tablets, for oral use, [CV in USA] - FOR EXPORT ONLY
Initial U.S. Approval: 2020

PACKAGE LABEL - REYVOW 50 mg 4ct carton - FOR EXPORT ONLY

NDC 0002-0265-04

4 tablets (1 card of 4 tablets)

REYVOW™

(lasmiditan)

tablets 50 mg

For oral use.

Each tablet contains 50 mg of lasmiditan.

Rx only

50 mg

Dispense enclosed Medication Guide to each patient.

Lilly

PDP Text – REYVOW 50 mg 8ct carton - FOR EXPORT ONLY

PACKAGE LABEL - REYVOW 100 mg 4ct carton - FOR EXPORT ONLY

NDC 0002-0632-04

4 tablets (1 card of 4 tablets)

REYVOW™

(lasmiditan)

tablets 100 mg

For oral use.

Each tablet contains 100 mg of lasmiditan.

Rx only

100 mg

Dispense enclosed Medication Guide to each patient.

Lilly

PDP Text – REYVOW 100 mg carton - FOR EXPORT ONLY
REYVOW 
lasmiditan tablet
Product Information
Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:0002-0265
Route of AdministrationORALDEA ScheduleCV    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
lasmiditan (UNII: 760I9WM792) (lasmiditan - UNII:760I9WM792) lasmiditan50 mg
Inactive Ingredients
Ingredient NameStrength
Microcrystalline cellulose (UNII: OP1R32D61U)  
Starch, corn (UNII: O8232NY3SJ)  
Croscarmellose Sodium (UNII: M28OL1HH48)  
Sodium Lauryl Sulfate (UNII: 368GB5141J)  
Magnesium Stearate (UNII: 70097M6I30)  
Polyvinyl Alcohol, Unspecified (UNII: 532B59J990)  
Titanium dioxide (UNII: 15FIX9V2JP)  
Polyethylene Glycol 3350 (UNII: G2M7P15E5P)  
Talc (UNII: 7SEV7J4R1U)  
Ferrosoferric Oxide (UNII: XM0M87F357)  
Product Characteristics
Colorgray (light gray) Scoreno score
ShapeOVAL (oval) Size9mm
FlavorImprint Code L50;4312
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:0002-0265-041 in 1 CARTON08/21/2020
14 in 1 BLISTER PACK; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
Export only08/21/2020
REYVOW 
lasmiditan tablet
Product Information
Product TypeHUMAN PRESCRIPTION DRUGItem Code (Source)NDC:0002-0632
Route of AdministrationORALDEA ScheduleCV    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
lasmiditan (UNII: 760I9WM792) (lasmiditan - UNII:760I9WM792) lasmiditan100 mg
Inactive Ingredients
Ingredient NameStrength
Microcrystalline cellulose (UNII: OP1R32D61U)  
Starch, corn (UNII: O8232NY3SJ)  
Croscarmellose Sodium (UNII: M28OL1HH48)  
Sodium Lauryl Sulfate (UNII: 368GB5141J)  
Magnesium Stearate (UNII: 70097M6I30)  
Polyvinyl Alcohol, Unspecified (UNII: 532B59J990)  
Titanium dioxide (UNII: 15FIX9V2JP)  
Polyethylene Glycol 3350 (UNII: G2M7P15E5P)  
Talc (UNII: 7SEV7J4R1U)  
Ferrosoferric Oxide (UNII: XM0M87F357)  
Ferric Oxide Red (UNII: 1K09F3G675)  
Product Characteristics
Colorpurple (light purple) Scoreno score
ShapeOVALSize12mm
FlavorImprint Code L100;4491
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:0002-0632-041 in 1 CARTON08/21/2020
14 in 1 BLISTER PACK; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
Export only08/21/2020
Labeler - Eli Lilly and Company (006421325)

Revised: 1/2023
Document Id: 00ae6b78-886a-468e-926e-f413df7867bf
Set id: 4da4eece-c3eb-4b2a-ae9e-7d040b29a334
Version: 2
Effective Time: 20230109
 
Eli Lilly and Company