NDC codes

FDA NDC Directory
Product NDC (as listed)85766-243Labeler and product segments. Claims need a package NDC.
Product NDC at billing width85766-0243Add the package segment from the table below.
Package NDCs as listed with the FDA, and the 11-digit 5-4-2 form used on claims. The highlighted digit is the added leading zero.
Package NDC11-digit (billing)PackageCopy
85766-243-0185766024301100 TABLET, FILM COATED in 1 BOTTLE (85766-243-01)Marketed from Jul 13, 2026
85766-243-208576602432020 TABLET, FILM COATED in 1 BOTTLE (85766-243-20)Marketed from Jul 21, 2026
85766-243-308576602433030 TABLET, FILM COATED in 1 BOTTLE (85766-243-30)Marketed from Jul 13, 2026
85766-243-998576602439910 BLISTER PACK in 1 CARTON (85766-243-99) / 10 TABLET, FILM COATED in 1 BLISTER PACKMarketed from Jul 13, 2026

How the 11-digit form is made: The product segment has 3 digits, so one leading zero is added to it (5-3-2 → 5-4-2). Formatting the NDC does not by itself make it billable — the product, package and quantity must match what was dispensed or administered, and payer rules apply. Conversion rules

Product information

Brand name (proprietary)
Journavx
Generic name (nonproprietary)
suzetrigine
Active ingredients
Suzetrigine — 50 mg/1
Dosage form
Tablet, Film coated
Route
Oral
Labeler
Sportpharm LLCNDC labeler code 85766
Product type
Prescription drug
Marketing category
NDA — New Drug ApplicationApplication NDA 219209
Marketing start
Listing expires
Other FDA classes
Cytochrome P450 3A Inducers (Mechanism)Sodium Channel Antagonists (Mechanism)
Identifiers
Product ID 85766-243_57223f5a-370d-d9d6-e063-6394a90ab906SPL ID 57223f5a-370d-d9d6-e063-6394a90ab906SPL set ID d229cf71-96ec-4206-960b-d56fafc250acRxCUI 2704833, 2704839UNII LOG73M21H5
Pharmacologic class
Sodium Channel Blocker

Billing references

What Med-Code can say about coding this product, and where each statement comes from. Nothing here is inferred from the name alone.

HCPCS codeNo match

No HCPCS code in Med-Code's directory. Oral products like this are usually dispensed by a pharmacy and billed by NDC.

NDC on a medical claim

N485766024301 followed by a unit qualifier and the quantity

Package 85766-0243-01. Unit qualifiers: F2 (international unit), GR (gram), ME (milligram), ML (milliliter), UN (unit (each)). The qualifier and quantity depend on what was given. About the N4 qualifier

Product label

Current FDA label (SPL), effective .

Indications (excerpt from the label)

JOURNAVX is indicated for the treatment of moderate to severe acute pain, including postoperative pain, in adults. JOURNAVX is a sodium channel blocker indicated for the treatment of moderate to severe acute pain, including postoperative pain, in adults. ( 1 )

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 85766-243

What is NDC 85766-243?
85766-243 is the product NDC for Journavx (suzetrigine), Suzetrigine 50 mg/1 tablet, film coated, listed with the FDA by Sportpharm LLC. It has 4 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Journavx (Suzetrigine).
What is the active ingredient?
Suzetrigine.
Who is the labeler?
Sportpharm LLC, NDC labeler code 85766. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Journavx?
1 other product NDC are listed under this name. See all Journavx NDCs.
Is there a related HCPCS / J-code?
Not in Med-Code's curated HCPCS directory. See Billing references above.

Other finished products listed under the same name: strengths, forms and labelers.

Other Journavx NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
JournavxsuzetrigineSuzetrigine 50 mg/1Tablet, Film coatedOralVertex Pharmaceuticals Incorporated51167-54851167-0548-2551167-0548-3051167-0548-31+1 more

Other NDCs under NDA 219209

Products listed under the same FDA application: other strengths and forms, and repackagers who relabel the same product.

FDA NDC Directory listings under NDA 219209
ProductStrengthForm · routeLabelerProduct NDC
JournavxsuzetrigineSuzetrigine 50 mg/1Tablet, Film coatedOralVertex Pharmaceuticals Incorporated51167-548

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