NDC 83703-536 - 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
83703-536
Package NDCs from labels
83703-536-20, 83703-536-01
Manufacturer
Bamboo US Bidco LCC | Baxter Deutschland GmbH
Effective date
2024-07-22
Current FDA listing
Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
LabelManufacturerEffective dateType
IFOSFAMIDE - Bamboo US Bidco LCC | Baxter Deutschland GmbHBamboo US Bidco LCC | Baxter Deutschland GmbH2024-07-22HUMAN PRESCRIPTION DRUG LABEL

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 7 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
IfosfamideIFOSFAMIDE FOR INJECTIONSteriMax Inc.98798c5e-8384-4990-a1b5-60dfb1e667bb2026-09-01Exact identifier
unii: UM20QQM95Y
IfosfamideIFOSFAMIDEFresenius Kabi USA, LLCa311a947-7b78-4226-bfe0-f4aa0be20e272026-04-09Boxed warning, Warnings, Adverse reactionsExact identifier
unii: UM20QQM95Y
IFEXIFOSFAMIDEBaxter Healthcare Corporationb7241707-7538-4d1a-91e7-3a25a91e0b9a2024-12-02Boxed warning, Warnings, Adverse reactionsExact identifier
unii: UM20QQM95Y
IFOSFAMIDEIFOSFAMIDEBaxter Healthcare Company91e433a9-6800-43a6-ac13-a49a04a5aecd2024-12-02Boxed warning, Warnings, Adverse reactionsExact identifier
unii: UM20QQM95Y
IFOSFAMIDEIFOSFAMIDEBaxter Healthcare Companyefb1d03b-2d91-406e-8110-d3a58b8fa7cc2024-12-02Boxed warning, Warnings, Adverse reactionsExact identifier
unii: UM20QQM95Y
1dd6b738-06aa-7279-e063-6394a90ab6fc1dd6bff7-e080-4b48-e063-6294a90abf7e2024-07-22Boxed warning, Warnings, Adverse reactionsExact identifier
spl id: 1dd6b738-06aa-7279-e063-6394a90ab6fc
spl set id: 1dd6bff7-e080-4b48-e063-6294a90abf7e
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.