NDC codes

FDA NDC Directory
Product NDC (as listed)50474-700Labeler and product segments. Claims need a package NDC.
Product NDC at billing width50474-0700Add 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
50474-700-61504740700612 KIT in 1 CARTON (50474-700-61) / 1 KIT in 1 KIT * 1 mL in 1 VIAL, GLASS * 1 mL in 1 VIAL, GLASSMarketed from Apr 20, 2008 · Sample package
50474-700-62504740700622 KIT in 1 CARTON (50474-700-62) / 1 KIT in 1 KIT * 1 mL in 1 VIAL, GLASS * 1 mL in 1 VIAL, GLASSMarketed from Apr 20, 2008

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)
Cimzia
Generic name (nonproprietary)
certolizumab pegol
Dosage form
Kit
Labeler
UCB, Inc.
Product type
Prescription drug
Marketing category
BLA — Biologics License ApplicationApplication BLA 125160
Marketing start
Listing expires
Identifiers
Product ID 50474-700_4b984e6f-72ac-4fdc-e063-6394a90af105SPL ID 4b984e6f-72ac-4fdc-e063-6394a90af105SPL set ID b4c2c9dc-a0bb-4d64-a667-a67ebe88392dRxCUI 795081, 795085, 849597, 849599, 2724369, 2724370, 2724371, 2724372UNII UMD07X179E

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.

NDC on a medical claim

N450474070061 followed by a unit qualifier and the quantity

Package 50474-0700-61. 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 . This label includes a boxed warning.

Indications (excerpt from the label)

CIMZIA is a tumor necrosis factor (TNF) blocker indicated for: Reducing signs and symptoms of Crohn's disease and maintaining clinical response in adult patients with moderately to severely active disease who have had an inadequate response to conventional therapy ( 1.1 ) Treatment of adults with moderately to severely active rheumatoid arthritis ( 1.2 ) Treatment of active polyarticular juvenile idiopathic arthritis (pJIA) in patients 2 years of age and older ( 1.3 ) Treatment of adult patients with active psoriatic arthritis. ( 1.4 ) Treatment of adults with active ankylosing spondylitis ( 1.5 ) Treatment of adults with active non-radiographic axial spondyloarthritis with objective signs o…

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under BLA 125160

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

FDA NDC Directory listings under BLA 125160
ProductStrengthForm · routeLabelerProduct NDC
Cimziacertolizumab pegolCertolizumab pegol 200 mg/mLInjection, SolutionSubcutaneousUCB, Inc.50474-710
Cimziacertolizumab pegolCertolizumab pegol 200 mg/mLInjection, SolutionSubcutaneousUCB, Inc.50474-750

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