NDC codes

FDA NDC Directory
Product NDC (as listed)50090-7769Labeler and product segments. Claims need a package NDC.
Product NDC at billing width50090-7769Add 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
50090-7769-050090776900500907769001 TRAY in 1 CARTON (50090-7769-0) / 1 mL in 1 TRAYMarketed from Nov 17, 2025

How the 11-digit form is made: The package segment has 1 digit, so one leading zero is added to it (5-4-1 → 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)
Selarsdi
Generic name (nonproprietary)
ustekinumab-aekn
Active ingredients
Ustekinumab — 90 mg/mL
Dosage form
Injection, Solution
Route
Subcutaneous
Labeler
A-S Medication SolutionsNDC labeler code 50090
Product type
Prescription drug
Marketing category
BLA — Biologics License ApplicationApplication BLA 761343
Marketing start
Listing expires
Other FDA classes
Interleukin-12 Antagonists (Mechanism)Interleukin-23 Antagonists (Mechanism)
Identifiers
Product ID 50090-7769_81578a89-3268-4b46-8cf7-79af3145f247SPL ID 81578a89-3268-4b46-8cf7-79af3145f247SPL set ID b3b483f4-3426-4d6d-97ae-39848ec1bfaeRxCUI 2705400, 2705401UNII FU77B4U5Z0
Pharmacologic class
Interleukin-12 Antagonist; Interleukin-23 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 codeMed-Code curated

J3357 — Injection, ustekinumab, for subcutaneous injection, 1 mg

Billing unit: 1 mg. Units on the claim = dose given ÷ 1 mg.

J3357 covers the subcutaneous formulation. The intravenous formulation has a separate code (J3358). Ustekinumab biosimilars are listed under their own names.

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

N450090776900 followed by a unit qualifier and the quantity

Package 50090-7769-00. 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)

SELARSDI is a human interleukin-12 and -23 antagonist indicated for the treatment of: Adult patients with: moderate to severe plaque psoriasis (PsO) who are candidates for phototherapy or systemic therapy. ( 1.1 ) active psoriatic arthritis (PsA) . ( 1.2 ) moderately to severely active Crohn’s disease (CD). ( 1.3 ) moderately to severely active ulcerative colitis. ( 1.4 ) Pediatric patients 6 years and older with: moderate to severe plaque psoriasis, who are candidates for phototherapy or systemic therapy. ( 1.1 ) active psoriatic arthritis (PsA) . ( 1.2 ) 1.1 Plaque Psoriasis (PsO) SELARSDI™ is indicated for the treatment of adults and pediatric patients 6 years of age and older with modera…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 50090-7769

What is NDC 50090-7769?
50090-7769 is the product NDC for Selarsdi (ustekinumab-aekn), Ustekinumab 90 mg/mL injection, solution, listed with the FDA by A-S Medication Solutions. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Selarsdi (Ustekinumab-aekn).
What is the active ingredient?
Ustekinumab.
Who is the labeler?
A-S Medication Solutions, NDC labeler code 50090. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Selarsdi?
3 other product NDCs are listed under this name. See all Selarsdi NDCs.
Is there a related HCPCS / J-code?
Yes: J3357, Injection, ustekinumab, for subcutaneous injection, 1 mg. See Billing references above.

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

Other Selarsdi NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
Selarsdiustekinumab-aeknUstekinumab-aekn 45 mg/.5mLInjection, SolutionSubcutaneousTeva Pharmaceuticals USA, Inc.51759-50551759-0505-1351759-0505-32
Selarsdiustekinumab-aeknUstekinumab-aekn 90 mg/mLInjection, SolutionSubcutaneousTeva Pharmaceuticals USA, Inc.51759-60751759-0607-32
Selarsdiustekinumab-aeknUstekinumab-aekn 130 mg/26mLInjection, SolutionIntravenousTeva Pharmaceuticals USA, Inc.51759-70851759-0708-13

Other NDCs under BLA 761343

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

FDA NDC Directory listings under BLA 761343
ProductStrengthForm · routeLabelerProduct NDC
Selarsdiustekinumab-aeknUstekinumab-aekn 45 mg/.5mLInjection, SolutionSubcutaneousTeva Pharmaceuticals USA, Inc.51759-505
Selarsdiustekinumab-aeknUstekinumab-aekn 90 mg/mLInjection, SolutionSubcutaneousTeva Pharmaceuticals USA, Inc.51759-607
Selarsdiustekinumab-aeknUstekinumab-aekn 130 mg/26mLInjection, SolutionIntravenousTeva Pharmaceuticals USA, Inc.51759-708
Ustekinumab-aeknUstekinumab-aekn 45 mg/.5mLInjection, SolutionSubcutaneousTeva Pharmaceuticals USA, Inc.51759-413
Ustekinumab-aeknUstekinumab-aekn 90 mg/mLInjection, SolutionSubcutaneousTeva Pharmaceuticals USA, Inc.51759-414
Ustekinumab-aeknUstekinumab-aekn 45 mg/.5mLInjection, SolutionSubcutaneousTeva Pharmaceuticals USA, Inc.51759-709
Ustekinumab-aeknUstekinumab-aekn 90 mg/mLInjection, SolutionSubcutaneousTeva Pharmaceuticals USA, Inc.51759-710

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