JOURNAVX

Product NDC
85766-243
Requested package NDC
85766-243-30
11-digit product format
857660243
Labeler code
85766
Product ID
85766-243_57223f5a-370d-d9d6-e063-6394a90ab906
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Suzetrigine
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
Sportpharm LLC
Application
NDA219209
Marketing category
NDA
Marketing start
2025-01-30
Substance
SUZETRIGINE
Active strength
50 mg/1
Pharmacologic classes
Cytochrome P450 3A Inducers [MoA], Sodium Channel Antagonists [MoA], Sodium Channel Blocker [EPC]
NDC exclude flag
No
Listing certified through
2027-12-31
Current FDA listing
Yes

Source provenance: Browse the complete Orange Book source catalog · source snapshot 43.

Orange Book products#

Current product rows page 1 of 1 · 1 matching rows.

Application-product, Trade name, Ingredient table
Application-productTrade nameIngredientStrengthDosage form / routeTE codesRLD / RSApproval date
N219209-001JOURNAVXSUZETRIGINE50MGTABLET / ORALRLD, RS2025-01-30

Orange Book patents#

Current patent rows page 1 of 1 · 1 matching rows.

Application-product, Patent, Expiration table
Application-productPatentExpirationUse codeCoverage / statusSubmission date
N219209-001118344412040-12-04U-4125Drug substance, Drug product2025-02-20

Orange Book exclusivity#

Current exclusivity rows page 1 of 1 · 1 matching rows.

Application-product, Exclusivity code, Expiration table
Application-productExclusivity codeExpiration
N219209-001NCE2030-01-30

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.

Captured, Edition, Application-product table
CapturedEditionApplication-productTrade nameStrengthDosage form / routeProduct TE source textRLD / RSApproval dateSource SHA-256
2026-09-14 22:38:342026-08N219209-001JOURNAVX50MGTABLET / ORALRLD, RS2025-01-3084e616aacf4f…
2026-08-18 06:07:402026-07N219209-001JOURNAVX50MGTABLET / ORALRLD, RS2025-01-30caaa826d4ba7…
2026-02-19 14:30 UTC2026-02N219209-001JOURNAVX50MGTABLET / ORALRLD, RS2025-01-30011fe1cb6892…
2025-12-14 10:44 UTC · 2 captures of this ZIP2025-12N219209-001JOURNAVX50MGTABLET / ORALRLD, RS2025-01-3031067a03dcf5…
2025-08-23 18:47 UTC2025-08N219209-001JOURNAVX50MGTABLET / ORALRLD, RS2025-01-306a471c1ec25d…
2025-03-22 03:13 UTC · 3 captures of this ZIP2025-03N219209-001JOURNAVX50MGTABLET / ORALRLD, RS2025-01-30fd3edfee7708…
2025-02-26 10:13 UTC · 3 captures of this ZIP2025-02N219209-001JOURNAVX50MGTABLET / ORALRLD, RS2025-01-30b8a1b40f171c…
2026-07-26 02:55 UTC · 3 captures of this ZIP2026-06N219209-001JOURNAVX50MGTABLET / ORALRLD, RS2025-01-30a50c72e98297…

Observed Orange Book patent history#

Captured, Edition, Application-product table
CapturedEditionApplication-productPatentExpirationUse codeCoverage / statusSubmission dateSource SHA-256
2026-09-14 22:38:342026-08N219209-001118344412040-12-04U-4125Drug substance, Drug product2025-02-2084e616aacf4f…
2026-08-18 06:07:402026-07N219209-001118344412040-12-04U-4125Drug substance, Drug product2025-02-20caaa826d4ba7…
2026-02-19 14:30 UTC2026-02N219209-001118344412040-12-04U-4125Drug substance, Drug product2025-02-20011fe1cb6892…
2025-12-14 10:44 UTC · 2 captures of this ZIP2025-12N219209-001118344412040-12-04U-4125Drug substance, Drug product2025-02-2031067a03dcf5…
2025-08-23 18:47 UTC2025-08N219209-001118344412040-12-04U-4125Drug substance, Drug product2025-02-206a471c1ec25d…
2025-03-22 03:13 UTC · 3 captures of this ZIP2025-03N219209-001118344412040-12-04U-4125Drug substance, Drug product2025-02-20fd3edfee7708…
2026-07-26 02:55 UTC · 3 captures of this ZIP2026-06N219209-001118344412040-12-04U-4125Drug substance, Drug product2025-02-20a50c72e98297…

Observed Orange Book exclusivity history#

Captured, Edition, Application-product table
CapturedEditionApplication-productExclusivity codeExpirationSource SHA-256
2026-09-14 22:38:342026-08N219209-001NCE2030-01-3084e616aacf4f…
2026-08-18 06:07:402026-07N219209-001NCE2030-01-30caaa826d4ba7…
2026-02-19 14:30 UTC2026-02N219209-001NCE2030-01-30011fe1cb6892…
2025-12-14 10:44 UTC · 2 captures of this ZIP2025-12N219209-001NCE2030-01-3031067a03dcf5…
2025-08-23 18:47 UTC2025-08N219209-001NCE2030-01-306a471c1ec25d…
2025-03-22 03:13 UTC · 3 captures of this ZIP2025-03N219209-001NCE2030-01-30fd3edfee7708…
2026-07-26 02:55 UTC · 3 captures of this ZIP2026-06N219209-001NCE2030-01-30a50c72e98297…

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.

Additional Listing Data#

Finished product
Yes
Brand name base
JOURNAVX
Listing expiration
2027-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
SUZETRIGINE50 mg/1

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
LOG73M21H5Internal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 2 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
2704833Internal RxNorm lookup
2704839Internal RxNorm lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
IdentifierFDA.report destination
d229cf71-96ec-4206-960b-d56fafc250acAvailable on FDA.report

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 · 2 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
JOURNAVXSUZETRIGINESportpharm LLCd229cf71-96ec-4206-960b-d56fafc250ac2026-07-21Warnings, Adverse reactionsExact identifier
application applno (NDA): 219209
application number: NDA219209
ndc (package): 85766-243-30
ndc (product): 85766-243
ndc11 (package): 85766024330
JOURNAVXSUZETRIGINEVertex Pharmaceuticals Incorporatedf0976da4-1d20-4517-945c-b60ed2f41c122026-04-13Warnings, Adverse reactionsExact identifier
application applno (NDA): 219209
application number: NDA219209

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startSampleExclude flagStatus
85766-243-308576602433030 TABLET, FILM COATED in 1 BOTTLE (85766-243-30) 2026-07-13NoNoCurrent