NDC codes

FDA NDC Directory
Product NDC (as listed)0002-5240Labeler and product segments. Claims need a package NDC.
Product NDC at billing width00002-5240Add 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
0002-5240-11000025240111 SYRINGE in 1 CARTON (0002-5240-11) / 3 mL in 1 SYRINGE (0002-5240-01)Marketed from Sep 23, 2026

How the 11-digit form is made: The labeler segment has 4 digits, so one leading zero is added to it (4-4-2 → 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)
ONSWIK KwikPenSuffix: KwikPen
Generic name (nonproprietary)
insulin efsitora alfa-gobe
Active ingredients
Insulin efsitora alfa — 1000 [iU]/mL
Dosage form
Injection, Solution
Route
Subcutaneous
Labeler
Eli Lilly and CompanyNDC labeler code 0002
Product type
Prescription drug
Marketing category
BLA — Biologics License ApplicationApplication BLA 761408
Marketing start
Listing expires
Identifiers
Product ID 0002-5240_da30dc98-a2dc-4a7c-91e1-180ca496daa4SPL ID da30dc98-a2dc-4a7c-91e1-180ca496daa4

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

N400002524011 followed by a unit qualifier and the quantity

Package 00002-5240-11. 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

The FDA listing for this product does not reference a label (SPL) set.

About NDC 0002-5240

What is NDC 0002-5240?
0002-5240 is the product NDC for ONSWIK KwikPen (insulin efsitora alfa-gobe), Insulin efsitora alfa 1000 [iU]/mL injection, solution, listed with the FDA by Eli Lilly and Company. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
ONSWIK KwikPen (Insulin efsitora alfa-gobe).
What is the active ingredient?
Insulin efsitora alfa.
Who is the labeler?
Eli Lilly and Company, NDC labeler code 0002. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for ONSWIK KwikPen?
1 other product NDC are listed under this name. See all ONSWIK KwikPen 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 ONSWIK KwikPen NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
ONSWIK KwikPeninsulin efsitora alfa-gobeInsulin efsitora alfa 500 [iU]/mLInjection, SolutionSubcutaneousEli Lilly and Company0002-513700002-5137-11

Other NDCs under BLA 761408

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

FDA NDC Directory listings under BLA 761408
ProductStrengthForm · routeLabelerProduct NDC
ONSWIK KwikPeninsulin efsitora alfa-gobeInsulin efsitora alfa 500 [iU]/mLInjection, SolutionSubcutaneousEli Lilly and Company0002-5137

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