NDC 10019-929-60 - IFOSFAMIDE

This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.

Product NDC
10019-929
Requested NDC
10019-929-60
Package NDCs from labels
10019-929-60, 10019-929-03
Manufacturer
Baxter Healthcare Company | Baxter Deutschland GmbH
Effective date
2024-12-02
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
IFOSFAMIDE - Baxter Healthcare Company | Baxter Deutschland GmbHBaxter Healthcare Company | Baxter Deutschland GmbH2024-12-02HUMAN PRESCRIPTION DRUG LABEL

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
10019-929-03IFOSFAMIDE1 in 1 CARTONINJECTION, POWDER, FOR SOLUTION111
10019-929-60IFOSFAMIDE60 mL in 1 VIALINJECTION, POWDER, FOR SOLUTION6011

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
10019-929IFOSFAMIDE INJECTION, POWDER, FOR SOLUTION [BAXTER HEALTHCARE CORPORATION]10Current NDC, Legacy NDC, 2 package rows20250213_efb1d03b-2d91-406e-8110-d3a58b8fa7cc.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
10019-929-03EA - Each10019-9297045d250-4a05-49d8-a19d-2da232efbe1a12019-02-13
10019-929-60EA - Each10019-929625ff536-80c1-462d-bca8-42eb1ae99bd912019-02-13

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 ยท 6 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
IfosfamideIFOSFAMIDE FOR INJECTIONSteriMax Inc.98798c5e-8384-4990-a1b5-60dfb1e667bb2026-09-01Exact identifier
rxcui: 1791593
unii: UM20QQM95Y
IfosfamideIFOSFAMIDEFresenius Kabi USA, LLCa311a947-7b78-4226-bfe0-f4aa0be20e272026-04-09Boxed warning, Warnings, Adverse reactionsExact identifier
rxcui: 1791593
unii: UM20QQM95Y
IFEXIFOSFAMIDEBaxter Healthcare Corporationb7241707-7538-4d1a-91e7-3a25a91e0b9a2024-12-02Boxed warning, Warnings, Adverse reactionsExact identifier
application number: NDA019763
rxcui: 1791588
rxcui: 1791593
unii: UM20QQM95Y
IFOSFAMIDEIFOSFAMIDEBaxter Healthcare Company91e433a9-6800-43a6-ac13-a49a04a5aecd2024-12-02Boxed warning, Warnings, Adverse reactionsExact identifier
application number: NDA019763
rxcui: 1791588
rxcui: 1791593
unii: UM20QQM95Y
IFOSFAMIDEIFOSFAMIDEBaxter Healthcare Companyefb1d03b-2d91-406e-8110-d3a58b8fa7cc2024-12-02Boxed warning, Warnings, Adverse reactionsExact identifier
application number: NDA019763
ndc (package): 10019-929-03
ndc (package): 10019-927-20
ndc (package): 10019-927-01
ndc (package): 10019-929-60
ndc (product): 10019-927
ndc (product): 10019-929
ndc11 (package): 10019092960
rxcui: 1791588
rxcui: 1791593
spl id: df9e4e92-2910-4268-9d98-44ab1fd6e47e
spl set id: efb1d03b-2d91-406e-8110-d3a58b8fa7cc
unii: UM20QQM95Y
IfosfamideIFOSFAMIDEHikma Pharmaceuticals USA Inc.c90ab05f-8fe5-437e-a1c0-8b11ef63291e2020-06-01Boxed warning, Warnings, Adverse reactionsExact identifier
unii: UM20QQM95Y

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.