NDC codes

FDA NDC Directory
Product NDC (as listed)55513-207Labeler and product segments. Claims need a package NDC.
Product NDC at billing width55513-0207Add 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
55513-207-01555130207011 VIAL in 1 CARTON (55513-207-01) / 16 mL in 1 VIALMarketed from Jun 1, 2018
55513-207-21555130207211 VIAL in 1 CARTON (55513-207-21) / 16 mL in 1 VIALMarketed from Jun 27, 2025

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)
Mvasi
Generic name (nonproprietary)
bevacizumab-awwb
Active ingredients
Bevacizumab — 400 mg/16mL
Dosage form
Injection, Solution
Route
Intravenous
Labeler
Amgen, Inc
Product type
Prescription drug
Marketing category
BLA — Biologics License ApplicationApplication BLA 761028
Marketing start
Listing expires
Other FDA classes
Vascular Endothelial Growth Factor Inhibitors (Mechanism)Vascular Endothelial Growth Factor-directed Antibody Interactions (Mechanism)
Identifiers
Product ID 55513-207_ea079b8e-24b7-4e03-8340-8078f30f6d98SPL ID ea079b8e-24b7-4e03-8340-8078f30f6d98SPL set ID 0a562b4e-67ce-4bab-852c-d9ee71e55fb8RxCUI 2046140, 2046145, 2046148, 2046149UNII 2S9ZZM9Q9V
Pharmacologic class
Vascular Endothelial Growth Factor Inhibitor

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

J9035 — Injection, bevacizumab, 10 mg

Billing unit: 10 mg. Units on the claim = dose given ÷ 10 mg.

Bevacizumab biosimilars have their own HCPCS codes.

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

N455513020701 followed by a unit qualifier and the quantity

Package 55513-0207-01. 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)

MVASI is a vascular endothelial growth factor inhibitor indicated for the treatment of: Metastatic colorectal cancer, in combination with intravenous fluorouracil-based chemotherapy for first- or second-line treatment. ( 1.1 ) Metastatic colorectal cancer, in combination with fluoropyrimidine-irinotecan- or fluoropyrimidine-oxaliplatin-based chemotherapy for second-line treatment in patients who have progressed on a first-line bevacizumab product-containing regimen. ( 1.1 ) Limitations of Use : MVASI is not indicated for adjuvant treatment of colon cancer. ( 1.1 ) Unresectable, locally advanced, recurrent or metastatic non-squamous non-small cell lung cancer, in combination with carboplatin …

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

Other NDCs under BLA 761028

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

FDA NDC Directory listings under BLA 761028
ProductStrengthForm · routeLabelerProduct NDC
Mvasibevacizumab-awwbBevacizumab 100 mg/4mLInjection, SolutionIntravenousAmgen, Inc55513-206

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