Home NDC 0002-4736-08 Reyvow
Product NDC 0002-4736
Requested package NDC 0002-4736-08
11-digit product format 000024736
Labeler code 0002
Product ID 0002-4736_f22c3672-c15f-4235-964a-3bda17de53f7
Type HUMAN PRESCRIPTION DRUG
Nonproprietary name lasmiditan
Dosage form TABLET
Route ORAL
Labeler Eli Lilly and Company
Application NDA211280
Marketing category NDA
Marketing start 2020-12-18
Marketing end 0000-00-00
Substance LASMIDITAN
Active strength 200 mg/1
DEA schedule CV
NDC exclude flag No
Listing certified through 2022-12-31
Current FDA listing Historical FDA.report record
Observed NDC auxiliary status history# This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.
Historic NDC status page 1 of 1 · 12 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Snapshot, Source SHA-256 table Captured / source date Snapshot Source SHA-256 2025-12-14 17:58 UTC · source 2025-12-05 d630ba8d3edf…732f749b63fb…2025-08-27 00:01 UTC · source 2025-08-26 f5e01cc5f278…a2eaf40c39c3…2025-04-01 02:39 UTC · source 2025-03-31 2ef7874e63bc…57b86245f4fa…2025-03-28 20:22 UTC · source 2025-03-28 a1b67e2a42f9…c4cf2c586c0d…2025-03-22 03:12 UTC · source 2025-03-21 cfe11265f3b6…090c488252e2…2025-03-10 12:48 UTC · source 2025-03-10 cdf11ea48f46…ba0047e9e063…2025-02-02 03:52 UTC · source 2025-01-31 302b2466d912…e7b80fea0513…2025-01-20 13:05 UTC · source 2025-01-20 ed331223b511…672a5bd82f5f…2025-01-11 03:41 UTC · source 2025-01-10 0efc9e666f02…f202fb6c5f17…2024-11-09 02:27 UTC · source 2024-11-08 ad56d346431e…cc804d4bbf1e…2024-10-04 04:10 UTC · source 2024-10-03 367a005e9d99…383a685ebd0f…2024-07-10 04:00 UTC · source 2024-07-09 557ba5c1ecfa…9c80585c8c6e…
Source provenance: Browse the complete Orange Book source catalog · source snapshot 43 .
Orange Book products# Current product rows page 1 of 1 · 3 matching rows.
Application-product, Trade name, Ingredient table Application-product Trade name Ingredient Strength Dosage form / route TE codes RLD / RS Approval date N211280-001 REYVOW LASMIDITAN SUCCINATE EQ 50MG BASE TABLET / ORAL RLD 2020-01-31 N211280-002 REYVOW LASMIDITAN SUCCINATE EQ 100MG BASE TABLET / ORAL RLD 2020-01-31 N211280-003 REYVOW LASMIDITAN SUCCINATE EQ 200MG BASE TABLET / ORAL RLD 2020-12-18
Orange Book patents# Current patent rows page 1 of 1 · 11 matching rows.
Application-product, Patent, Expiration table Application-product Patent Expiration Use code Coverage / status Submission date N211280-001 7423050 2028-02-17 U-1719 Drug substance, Drug product 2020-02-25 N211280-001 12257246 2030-07-07 U-2718 2025-04-22 N211280-001 11053214 2037-12-05 U-1719 Drug substance, Drug product 2021-07-28 N211280-001 12071423 2040-07-06 Drug product 2024-09-20 N211280-002 7423050 2028-02-17 U-1719 Drug substance, Drug product 2020-02-25 N211280-002 12257246 2030-07-07 U-2718 2025-04-22 N211280-002 11053214 2037-12-05 U-1719 Drug substance, Drug product 2021-07-28 N211280-002 12071423 2040-07-06 Drug product 2024-09-20 N211280-003 7423050 2028-02-17 U-1719 Drug substance, Drug product 2021-07-28 N211280-003 12257246 2030-07-07 U-2718 2025-04-22 N211280-003 11053214 2037-12-05 U-1719 Drug substance, Drug product 2021-07-28
Observed Orange Book product history# Observed FDA ZIP history: Each table is queried independently by exact application/product key from successfully parsed Orange Book snapshots. Capture times identify archived source observations; absence or a change between snapshots is not inferred. FDA publication files that were not recoverable as structured ZIP data are not represented as states.
Product history page 1 of 3 · 115 observed states.
Captured, Edition, Application-product table Captured Edition Application-product Trade name Strength Dosage form / route Product TE source text RLD / RS Approval date Source SHA-256 2026-09-14 22:38:34 2026-08 N211280-001 REYVOW EQ 50MG BASE TABLET / ORAL RLD 2020-01-31 84e616aacf4f…2026-09-14 22:38:34 2026-08 N211280-002 REYVOW EQ 100MG BASE TABLET / ORAL RLD 2020-01-31 84e616aacf4f…2026-09-14 22:38:34 2026-08 N211280-003 REYVOW EQ 200MG BASE TABLET / ORAL RLD 2020-12-18 84e616aacf4f…2026-08-18 06:07:40 2026-07 N211280-001 REYVOW EQ 50MG BASE TABLET / ORAL RLD 2020-01-31 caaa826d4ba7…2026-08-18 06:07:40 2026-07 N211280-002 REYVOW EQ 100MG BASE TABLET / ORAL RLD 2020-01-31 caaa826d4ba7…2026-08-18 06:07:40 2026-07 N211280-003 REYVOW EQ 200MG BASE TABLET / ORAL RLD 2020-12-18 caaa826d4ba7…2026-02-19 14:30 UTC 2026-02 N211280-001 REYVOW EQ 50MG BASE TABLET / ORAL RLD 2020-01-31 011fe1cb6892…2026-02-19 14:30 UTC 2026-02 N211280-002 REYVOW EQ 100MG BASE TABLET / ORAL RLD, RS 2020-01-31 011fe1cb6892…2026-02-19 14:30 UTC 2026-02 N211280-003 REYVOW EQ 200MG BASE TABLET / ORAL RLD 2020-12-18 011fe1cb6892…2025-12-14 10:44 UTC · 2 captures of this ZIP 2025-12 N211280-001 REYVOW EQ 50MG BASE TABLET / ORAL RLD 2020-01-31 31067a03dcf5…2025-12-14 10:44 UTC · 2 captures of this ZIP 2025-12 N211280-002 REYVOW EQ 100MG BASE TABLET / ORAL RLD, RS 2020-01-31 31067a03dcf5…2025-12-14 10:44 UTC · 2 captures of this ZIP 2025-12 N211280-003 REYVOW EQ 200MG BASE TABLET / ORAL RLD 2020-12-18 31067a03dcf5…2025-08-23 18:47 UTC 2025-08 N211280-001 REYVOW EQ 50MG BASE TABLET / ORAL RLD 2020-01-31 6a471c1ec25d…2025-08-23 18:47 UTC 2025-08 N211280-002 REYVOW EQ 100MG BASE TABLET / ORAL RLD, RS 2020-01-31 6a471c1ec25d…2025-08-23 18:47 UTC 2025-08 N211280-003 REYVOW EQ 200MG BASE TABLET / ORAL RLD 2020-12-18 6a471c1ec25d…2025-03-22 03:13 UTC · 3 captures of this ZIP 2025-03 N211280-001 REYVOW EQ 50MG BASE TABLET / ORAL RLD 2020-01-31 fd3edfee7708…2025-03-22 03:13 UTC · 3 captures of this ZIP 2025-03 N211280-002 REYVOW EQ 100MG BASE TABLET / ORAL RLD, RS 2020-01-31 fd3edfee7708…2025-03-22 03:13 UTC · 3 captures of this ZIP 2025-03 N211280-003 REYVOW EQ 200MG BASE TABLET / ORAL RLD 2020-12-18 fd3edfee7708…2025-02-26 10:13 UTC · 3 captures of this ZIP 2025-02 N211280-001 REYVOW EQ 50MG BASE TABLET / ORAL RLD 2020-01-31 b8a1b40f171c…2025-02-26 10:13 UTC · 3 captures of this ZIP 2025-02 N211280-002 REYVOW EQ 100MG BASE TABLET / ORAL RLD, RS 2020-01-31 b8a1b40f171c…2025-02-26 10:13 UTC · 3 captures of this ZIP 2025-02 N211280-003 REYVOW EQ 200MG BASE TABLET / ORAL RLD 2020-12-18 b8a1b40f171c…2025-01-19 17:59 UTC · 7 captures of this ZIP 2025-01 N211280-001 REYVOW EQ 50MG BASE TABLET / ORAL RLD 2020-01-31 03ed91905a0d…2025-01-19 17:59 UTC · 7 captures of this ZIP 2025-01 N211280-002 REYVOW EQ 100MG BASE TABLET / ORAL RLD, RS 2020-01-31 03ed91905a0d…2025-01-19 17:59 UTC · 7 captures of this ZIP 2025-01 N211280-003 REYVOW EQ 200MG BASE TABLET / ORAL RLD 2020-12-18 03ed91905a0d…2024-12-13 21:23 UTC · 2 captures of this ZIP 2024-12 N211280-001 REYVOW EQ 50MG BASE TABLET / ORAL RLD 2020-01-31 2680178bc6a6…2024-12-13 21:23 UTC · 2 captures of this ZIP 2024-12 N211280-002 REYVOW EQ 100MG BASE TABLET / ORAL RLD, RS 2020-01-31 2680178bc6a6…2024-12-13 21:23 UTC · 2 captures of this ZIP 2024-12 N211280-003 REYVOW EQ 200MG BASE TABLET / ORAL RLD 2020-12-18 2680178bc6a6…2024-09-14 05:58 UTC · 2 captures of this ZIP 2024-09 N211280-001 REYVOW EQ 50MG BASE TABLET / ORAL RLD 2020-01-31 5bbf6a4d5a75…2024-09-14 05:58 UTC · 2 captures of this ZIP 2024-09 N211280-002 REYVOW EQ 100MG BASE TABLET / ORAL RLD, RS 2020-01-31 5bbf6a4d5a75…2024-09-14 05:58 UTC · 2 captures of this ZIP 2024-09 N211280-003 REYVOW EQ 200MG BASE TABLET / ORAL RLD 2020-12-18 5bbf6a4d5a75…2024-11-08 22:44 UTC · 3 captures of this ZIP 2024-11 N211280-001 REYVOW EQ 50MG BASE TABLET / ORAL RLD 2020-01-31 d8e5a09893c0…2024-11-08 22:44 UTC · 3 captures of this ZIP 2024-11 N211280-002 REYVOW EQ 100MG BASE TABLET / ORAL RLD, RS 2020-01-31 d8e5a09893c0…2024-11-08 22:44 UTC · 3 captures of this ZIP 2024-11 N211280-003 REYVOW EQ 200MG BASE TABLET / ORAL RLD 2020-12-18 d8e5a09893c0…2024-10-29 15:01 UTC 2024-10 N211280-001 REYVOW EQ 50MG BASE TABLET / ORAL RLD 2020-01-31 d06236e962d9…2024-10-29 15:01 UTC 2024-10 N211280-002 REYVOW EQ 100MG BASE TABLET / ORAL RLD, RS 2020-01-31 d06236e962d9…2024-10-29 15:01 UTC 2024-10 N211280-003 REYVOW EQ 200MG BASE TABLET / ORAL RLD 2020-12-18 d06236e962d9…2024-08-13 05:28 UTC · 3 captures of this ZIP 2024-08 N211280-001 REYVOW EQ 50MG BASE TABLET / ORAL RLD 2020-01-31 79d66fd596c7…2024-08-13 05:28 UTC · 3 captures of this ZIP 2024-08 N211280-002 REYVOW EQ 100MG BASE TABLET / ORAL RLD, RS 2020-01-31 79d66fd596c7…2024-08-13 05:28 UTC · 3 captures of this ZIP 2024-08 N211280-003 REYVOW EQ 200MG BASE TABLET / ORAL RLD 2020-12-18 79d66fd596c7…2024-07-13 05:37 UTC · 2 captures of this ZIP 2024-07 N211280-001 REYVOW EQ 50MG BASE TABLET / ORAL RLD 2020-01-31 301d65b070ca…
Observed Orange Book patent history# Patent history page 1 of 8 · 316 observed states.
Captured, Edition, Application-product table Captured Edition Application-product Patent Expiration Use code Coverage / status Submission date Source SHA-256 2026-09-14 22:38:34 2026-08 N211280-001 7423050 2028-02-17 U-1719 Drug substance, Drug product 2020-02-25 84e616aacf4f…2026-09-14 22:38:34 2026-08 N211280-001 12257246 2030-07-07 U-2718 2025-04-22 84e616aacf4f…2026-09-14 22:38:34 2026-08 N211280-001 11053214 2037-12-05 U-1719 Drug substance, Drug product 2021-07-28 84e616aacf4f…2026-09-14 22:38:34 2026-08 N211280-001 12071423 2040-07-06 Drug product 2024-09-20 84e616aacf4f…2026-09-14 22:38:34 2026-08 N211280-002 7423050 2028-02-17 U-1719 Drug substance, Drug product 2020-02-25 84e616aacf4f…2026-09-14 22:38:34 2026-08 N211280-002 12257246 2030-07-07 U-2718 2025-04-22 84e616aacf4f…2026-09-14 22:38:34 2026-08 N211280-002 11053214 2037-12-05 U-1719 Drug substance, Drug product 2021-07-28 84e616aacf4f…2026-09-14 22:38:34 2026-08 N211280-002 12071423 2040-07-06 Drug product 2024-09-20 84e616aacf4f…2026-09-14 22:38:34 2026-08 N211280-003 7423050 2028-02-17 U-1719 Drug substance, Drug product 2021-07-28 84e616aacf4f…2026-09-14 22:38:34 2026-08 N211280-003 12257246 2030-07-07 U-2718 2025-04-22 84e616aacf4f…2026-09-14 22:38:34 2026-08 N211280-003 11053214 2037-12-05 U-1719 Drug substance, Drug product 2021-07-28 84e616aacf4f…2026-08-18 06:07:40 2026-07 N211280-001 7423050 2028-02-17 U-1719 Drug substance, Drug product 2020-02-25 caaa826d4ba7…2026-08-18 06:07:40 2026-07 N211280-001 12257246 2030-07-07 U-2718 2025-04-22 caaa826d4ba7…2026-08-18 06:07:40 2026-07 N211280-001 11053214 2037-12-05 U-1719 Drug substance, Drug product 2021-07-28 caaa826d4ba7…2026-08-18 06:07:40 2026-07 N211280-001 12071423 2040-07-06 Drug product 2024-09-20 caaa826d4ba7…2026-08-18 06:07:40 2026-07 N211280-002 7423050 2028-02-17 U-1719 Drug substance, Drug product 2020-02-25 caaa826d4ba7…2026-08-18 06:07:40 2026-07 N211280-002 12257246 2030-07-07 U-2718 2025-04-22 caaa826d4ba7…2026-08-18 06:07:40 2026-07 N211280-002 11053214 2037-12-05 U-1719 Drug substance, Drug product 2021-07-28 caaa826d4ba7…2026-08-18 06:07:40 2026-07 N211280-002 12071423 2040-07-06 Drug product 2024-09-20 caaa826d4ba7…2026-08-18 06:07:40 2026-07 N211280-003 7423050 2028-02-17 U-1719 Drug substance, Drug product 2021-07-28 caaa826d4ba7…2026-08-18 06:07:40 2026-07 N211280-003 12257246 2030-07-07 U-2718 2025-04-22 caaa826d4ba7…2026-08-18 06:07:40 2026-07 N211280-003 11053214 2037-12-05 U-1719 Drug substance, Drug product 2021-07-28 caaa826d4ba7…2026-02-19 14:30 UTC 2026-02 N211280-001 7423050 2028-02-17 U-1719 Drug substance, Drug product 2020-02-25 011fe1cb6892…2026-02-19 14:30 UTC 2026-02 N211280-001 12257246 2030-07-07 U-2718 2025-04-22 011fe1cb6892…2026-02-19 14:30 UTC 2026-02 N211280-001 11053214 2037-12-05 U-1719 Drug substance, Drug product 2021-07-28 011fe1cb6892…2026-02-19 14:30 UTC 2026-02 N211280-001 12071423 2040-07-06 Drug product 2024-09-20 011fe1cb6892…2026-02-19 14:30 UTC 2026-02 N211280-002 7423050 2028-02-17 U-1719 Drug substance, Drug product 2020-02-25 011fe1cb6892…2026-02-19 14:30 UTC 2026-02 N211280-002 12257246 2030-07-07 U-2718 2025-04-22 011fe1cb6892…2026-02-19 14:30 UTC 2026-02 N211280-002 11053214 2037-12-05 U-1719 Drug substance, Drug product 2021-07-28 011fe1cb6892…2026-02-19 14:30 UTC 2026-02 N211280-002 12071423 2040-07-06 Drug product 2024-09-20 011fe1cb6892…2026-02-19 14:30 UTC 2026-02 N211280-003 7423050 2028-02-17 U-1719 Drug substance, Drug product 2021-07-28 011fe1cb6892…2026-02-19 14:30 UTC 2026-02 N211280-003 12257246 2030-07-07 U-2718 2025-04-22 011fe1cb6892…2026-02-19 14:30 UTC 2026-02 N211280-003 11053214 2037-12-05 U-1719 Drug substance, Drug product 2021-07-28 011fe1cb6892…2025-12-14 10:44 UTC · 2 captures of this ZIP 2025-12 N211280-001 7423050 2028-02-17 U-1719 Drug substance, Drug product 2020-02-25 31067a03dcf5…2025-12-14 10:44 UTC · 2 captures of this ZIP 2025-12 N211280-001 12257246 2030-07-07 U-2718 2025-04-22 31067a03dcf5…2025-12-14 10:44 UTC · 2 captures of this ZIP 2025-12 N211280-001 11053214 2037-12-05 U-1719 Drug substance, Drug product 2021-07-28 31067a03dcf5…2025-12-14 10:44 UTC · 2 captures of this ZIP 2025-12 N211280-001 12071423 2040-07-06 Drug product 2024-09-20 31067a03dcf5…2025-12-14 10:44 UTC · 2 captures of this ZIP 2025-12 N211280-002 7423050 2028-02-17 U-1719 Drug substance, Drug product 2020-02-25 31067a03dcf5…2025-12-14 10:44 UTC · 2 captures of this ZIP 2025-12 N211280-002 12257246 2030-07-07 U-2718 2025-04-22 31067a03dcf5…2025-12-14 10:44 UTC · 2 captures of this ZIP 2025-12 N211280-002 11053214 2037-12-05 U-1719 Drug substance, Drug product 2021-07-28 31067a03dcf5…
Observed Orange Book exclusivity history# Exclusivity history page 1 of 3 · 101 observed states.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 1 of 1 · 1 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Reyvow LASMIDITAN Eli Lilly and Company aea3358c-ff41-4490-9e6d-c7bf7b3de13f 2026-01-08 Warnings, Adverse reactions Exact identifier application applno (NDA): 211280 application number: NDA211280
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 0002-4736-08 00002473608 2 BLISTER PACK in 1 CARTON (0002-4736-08) > 4 TABLET in 1 BLISTER PACK 2 blister pack 2020-12-18 0000-00-00 No No Current