NDC codes

FDA NDC Directory
Product NDC (as listed)10019-929Labeler and product segments. Claims need a package NDC.
Product NDC at billing width10019-0929Add 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
10019-929-03100190929031 VIAL in 1 CARTON (10019-929-03) / 60 mL in 1 VIAL (10019-929-60)Marketed from Aug 2, 2018

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)
Ifosfamide
Generic name (nonproprietary)
ifosfamide
Active ingredients
Ifosfamide — 3 g/60mL
Dosage form
Injection, Powder, For solution
Route
Intravenous
Labeler
Baxter Healthcare CompanyNDC labeler code 10019
Product type
Prescription drug
Marketing category
NDA — New Drug ApplicationApplication NDA 019763
Marketing start
Listing expires
Other FDA classes
Alkylating Activity (Mechanism)
Identifiers
Product ID 10019-929_df9e4e92-2910-4268-9d98-44ab1fd6e47eSPL ID df9e4e92-2910-4268-9d98-44ab1fd6e47eSPL set ID efb1d03b-2d91-406e-8110-d3a58b8fa7ccRxCUI 1791588, 1791593UNII UM20QQM95Y
Pharmacologic class
Alkylating Drug

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

N410019092903 followed by a unit qualifier and the quantity

Package 10019-0929-03. 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)

Ifosfamide for Injection is indicated for use in adults in combination with certain other approved antineoplastic agents for third-line chemotherapy of germ cell testicular cancer. Ifosfamide for Injection is an alkylating drug indicated for use in adults in combination with certain other approved antineoplastic agents for third-line chemotherapy of germ cell testicular cancer.

Excerpt only. Read the full label for complete information.

Full label on DailyMed (opens in a new tab)

About NDC 10019-929

What is NDC 10019-929?
10019-929 is the product NDC for Ifosfamide, Ifosfamide 3 g/60mL injection, powder, for solution, listed with the FDA by Baxter Healthcare Company. It has 1 package NDC, shown above in 10- and 11-digit form.
What drug is associated with this NDC?
Ifosfamide.
What is the active ingredient?
Ifosfamide.
Who is the labeler?
Baxter Healthcare Company, NDC labeler code 10019. The labeler is the company responsible for the label; it may be the manufacturer, a repackager or a distributor.
What other NDCs exist for Ifosfamide?
7 other product NDCs are listed under this name. See all Ifosfamide 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 Ifosfamide NDCs
ProductStrengthForm · routeLabelerProduct NDCPackage NDCs (11-digit)
Ifosfamideifosfamide for injectionIfosfamide 1 g/1Powder, For solutionIntravenousSteriMax Inc.21586-21121586-0211-02
IfosfamideIfosfamide 50 mg/mLInjectionIntravenousHikma Pharmaceuticals USA Inc.0143-953000143-9530-01
IfosfamideIfosfamide 50 mg/mLInjectionIntravenousHikma Pharmaceuticals USA Inc.0143-953100143-9531-01
IfosfamideIfosfamide 1 g/1Injection, Powder, Lyophilized, For solutionIntravenousFresenius Kabi USA, LLC63323-14263323-0142-10
IfosfamideIfosfamide 1 g/20mLInjection, Powder, For solutionIntravenousBaxter Healthcare Company10019-92510019-0925-01
IfosfamideIfosfamide 3 g/60mLInjection, Powder, For solutionIntravenousBaxter Healthcare Company10019-92610019-0926-02
IfosfamideIfosfamide 1 g/20mLInjection, Powder, For solutionIntravenousBaxter Healthcare Company10019-92710019-0927-01

Other NDCs under NDA 019763

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

FDA NDC Directory listings under NDA 019763
ProductStrengthForm · routeLabelerProduct NDC
IfosfamideIfosfamide 1 g/20mLInjection, Powder, For solutionIntravenousBaxter Healthcare Company10019-925
IfosfamideIfosfamide 3 g/60mLInjection, Powder, For solutionIntravenousBaxter Healthcare Company10019-926
IfosfamideIfosfamide 1 g/20mLInjection, Powder, For solutionIntravenousBaxter Healthcare Company10019-927
IfexifosfamideIfosfamide 1 g/20mLInjection, Powder, For solutionIntravenousBaxter Healthcare Corporation0338-3991
IfexifosfamideIfosfamide 3 g/60mLInjection, Powder, For solutionIntravenousBaxter Healthcare Corporation0338-3993

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