NDC codes

FDA NDC Directory
Product NDC (as listed)50222-361Labeler and product segments. Claims need a package NDC.
Product NDC at billing width50222-0361Add 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
50222-361-02502220361022 SYRINGE, GLASS in 1 CARTON (50222-361-02) / 1 mL in 1 SYRINGE, GLASS (50222-361-11)Marketed from Mar 9, 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)
Spevigo
Generic name (nonproprietary)
spesolimab
Active ingredients
Spesolimab — 150 mg/mL
Dosage form
Injection
Route
Subcutaneous
Labeler
LEO Pharma Inc.NDC labeler code 50222
Product type
Prescription drug
Marketing category
BLA — Biologics License ApplicationApplication BLA 761244
Marketing start
Listing expires
Other FDA classes
Interleukin-36 Receptor Antagonists (Mechanism)
Identifiers
Product ID 50222-361_40cef378-e90e-4891-812a-b3c889dc9193SPL ID 40cef378-e90e-4891-812a-b3c889dc9193SPL set ID 78a4f7eb-8d34-4467-8d40-74ed24323806RxCUI 2610422, 2610428, 2678979, 2678984, 2716696, 2716697UNII 5IB2J79MCX
Pharmacologic class
Interleukin-36 Receptor Antagonist

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 drug-specific HCPCS code in Med-Code's directory for this product. The directory is curated and not complete — check the current CMS HCPCS file before billing.

Administration

Drug administration (CPT 96360–96549)

When a clinician administers the drug, the administration is reported separately. Codes in this range cover hydration, therapeutic injections and infusions, and chemotherapy or other complex drug administration. The right code depends on route, duration and drug type, and self-administered drugs are not billed this way.

How CPT relates to drug billing

NDC on a medical claim

N450222036102 followed by a unit qualifier and the quantity

Package 50222-0361-02. 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)

SPEVIGO is indicated for the treatment of generalized pustular psoriasis (GPP) in adults and pediatric patients 12 years of age and older and weighing at least 40 kg. SPEVIGO is an interleukin-36 receptor antagonist indicated for the treatment of generalized pustular psoriasis (GPP) in adults and pediatric patients 12 years of age and older and weighing at least 40 kg. ( 1 )

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 50222-361

What is NDC 50222-361?
50222-361 is the product NDC for Spevigo (spesolimab), Spesolimab 150 mg/mL injection, listed with the FDA by LEO Pharma Inc.. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Spevigo (Spesolimab).
What is the active ingredient?
Spesolimab.
Who is the labeler?
LEO Pharma Inc., NDC labeler code 50222. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Spevigo?
5 other product NDCs are listed under this name. See all Spevigo 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 Spevigo NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
SpevigospesolimabSpesolimab 300 mg/2mLInjectionSubcutaneousLEO Pharma Inc.50222-36250222-0362-0150222-0362-02
SpevigospesolimabSpesolimab 60 mg/mLInjectionSubcutaneousLEO Pharma Inc.50222-36050222-0360-72
Spevigospesolimab-sbzoSpesolimab 300 mg/1InjectionIntravenousBoehringer Ingelheim Pharmaceuticals, Inc.0597-770500597-7705-4100597-7705-72
Spevigospesolimab-sbzoSpesolimab 150 mg/1InjectionIntravenousBoehringer Ingelheim Pharmaceuticals, Inc.0597-062000597-0620-20
Spevigospesolimab-sbzoSpesolimab 60 mg/mLInjectionIntravenousBoehringer Ingelheim Pharmaceuticals, Inc.0597-003500597-0035-10

Other NDCs under BLA 761244

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

FDA NDC Directory listings under BLA 761244
ProductStrengthForm · routeLabelerProduct NDC
SpevigospesolimabSpesolimab 300 mg/2mLInjectionSubcutaneousLEO Pharma Inc.50222-362
SpevigospesolimabSpesolimab 60 mg/mLInjectionSubcutaneousLEO Pharma Inc.50222-360
Spevigospesolimab-sbzoSpesolimab 150 mg/1InjectionIntravenousBoehringer Ingelheim Pharmaceuticals, Inc.0597-0620
Spevigospesolimab-sbzoSpesolimab 300 mg/1InjectionIntravenousBoehringer Ingelheim Pharmaceuticals, Inc.0597-7705
Spevigospesolimab-sbzoSpesolimab 60 mg/mLInjectionIntravenousBoehringer Ingelheim Pharmaceuticals, Inc.0597-0035

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