NDC codes

FDA NDC Directory
Product NDC (as listed)25021-259Labeler and product segments. Claims need a package NDC.
Product NDC at billing width25021-0259Add 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
25021-259-5025021025950250210259501 VIAL in 1 CARTON (25021-259-50) / 50 mL in 1 VIALMarketed from Aug 1, 2024
25021-259-5125021025951250210259516 VIAL in 1 CARTON (25021-259-51) / 50 mL in 1 VIALMarketed from Aug 1, 2024

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)
Nelarabine
Generic name (nonproprietary)
nelarabine
Active ingredients
Nelarabine — 5 mg/mL
Dosage form
Injection, Solution
Route
Intravenous
Labeler
Sagent PharmaceuticalsNDC labeler code 25021
Product type
Prescription drug
Marketing category
ANDA — Abbreviated New Drug Application (generic)Application ANDA 212605
Marketing start
Listing expires
Other FDA classes
Nucleic Acid Synthesis Inhibitors (Mechanism)
Identifiers
Product ID 25021-259_c956537f-71c0-44bc-a2e2-ab2adaa4f756SPL ID c956537f-71c0-44bc-a2e2-ab2adaa4f756SPL set ID f60da70f-2f9e-421d-a277-95b1edb57a71RxCUI 603566UNII 60158CV180
Pharmacologic class
Nucleoside Metabolic 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 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

N425021025950 followed by a unit qualifier and the quantity

Package 25021-0259-50. 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)

Nelarabine is indicated for the treatment of T-cell acute lymphoblastic leukemia (T-ALL) and T-cell lymphoblastic lymphoma (T-LBL) in adult and pediatric patients age 1 year and older whose disease has not responded to or has relapsed following treatment with at least two chemotherapy regimens. Nelarabine is a nucleoside metabolic inhibitor indicated for the treatment of patients with T-cell acute lymphoblastic leukemia and T-cell lymphoblastic lymphoma in adult and pediatric patients age 1 year and older whose disease has not responded to or has relapsed following treatment with at least two chemotherapy regimens. ( 1 )

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 25021-259

What is NDC 25021-259?
25021-259 is the product NDC for Nelarabine, Nelarabine 5 mg/mL injection, solution, listed with the FDA by Sagent Pharmaceuticals. It has 2 package NDCs, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Nelarabine.
What is the active ingredient?
Nelarabine.
Who is the labeler?
Sagent Pharmaceuticals, NDC labeler code 25021. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Nelarabine?
13 other product NDCs are listed under this name. See all Nelarabine 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 Nelarabine NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
nelarabineNelarabine 5 mg/mLInjectionIntravenousShorla Oncology Inc.81927-37581927-0375-01
NelarabineNelarabine 5 mg/mLInjectionIntravenousXGen Pharmaceuticals DJB, Inc.39822-065039822-0650-0139822-0650-06
NelarabineNelarabine 5 mg/mLInjectionIntravenousNovadoz Pharmaceuticals LLC72205-15472205-0154-0172205-0154-04
NelarabineNelarabine 5 mg/mLInjectionIntravenousAlembic Pharmaceuticals Limited46708-81346708-0813-5046708-0813-63
NelarabineNelarabine 5 mg/mLInjectionIntravenousAlembic Pharmaceuticals Inc.62332-81362332-0813-5062332-0813-63
NelarabineNelarabine 5 mg/mLInjectionIntravenousGland Pharma Limited68083-23368083-0233-06
NelarabineNelarabine 5 mg/mLInjectionIntravenousAmneal Pharmaceuticals LLC70121-174370121-1743-0170121-1743-04
nelarabineNelarabine 5 mg/mLInjectionIntravenousShorla Oncology Inc.81927-11181927-0111-0181927-0111-06
NelarabineNelarabine 5 mg/mLInjectionIntravenousMeitheal Pharmaceuticals Inc71288-16571288-0165-54
NelarabineNelarabine 5 mg/mLInjectionIntravenousDr. Reddy's Laboratories, Inc.43598-14243598-0142-0643598-0142-11

All 14 Nelarabine NDCs

Other NDCs under ANDA 212605

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

FDA NDC Directory listings under ANDA 212605
ProductStrengthForm · routeLabelerProduct NDC
NelarabineNelarabine 5 mg/mLInjectionIntravenousGland Pharma Limited68083-233

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