ifosfamide

Generic: ifosfamide

Labeler: baxter healthcare corporation
NDC Directory HUMAN PRESCRIPTION DRUG NDA Inactive Finished

Drug Facts

Product Profile

Brand Name ifosfamide
Generic Name ifosfamide
Labeler baxter healthcare corporation
Dosage Form INJECTION, POWDER, FOR SOLUTION
Routes
INTRAVENOUS
Active Ingredients

ifosfamide 3 g/60mL

Manufacturer
Baxter Healthcare Corporation

Identifiers & Regulatory

Product NDC 10019-926
Product ID 10019-926_7fd51853-2c9b-4291-85a8-a8ebf8782a92
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number NDA019763
Listing Expiration 2026-12-31
Marketing Start 1988-12-30

Pharmacologic Class

Established (EPC)
alkylating drug [epc]
Mechanism of Action
alkylating activity [moa]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 10019926
Hyphenated Format 10019-926

Supplemental Identifiers

RxCUI
1791588 1791593
UNII
UM20QQM95Y
NUI
N0000000236 N0000175558

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name ifosfamide (source: ndc)
Generic Name ifosfamide (source: ndc)
Application Number NDA019763 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 3 g/60mL
source: ndc
Packaging
  • 1 VIAL, SINGLE-DOSE in 1 CARTON (10019-926-02) / 60 mL in 1 VIAL, SINGLE-DOSE (10019-926-16)
source: ndc

Packages (1)

10019-926-02 1 VIAL, SINGLE-DOSE in 1 CARTON (10019-926-02) / 60 mL in 1 VIAL, SINGLE-DOSE (10019-926-16)

Ingredients (1)

ifosfamide (3 g/60mL)

Linked Drug Pages (1)

IFOSFAMIDE ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAVENOUS"], "spl_id": "7fd51853-2c9b-4291-85a8-a8ebf8782a92", "openfda": {"nui": ["N0000000236", "N0000175558"], "unii": ["UM20QQM95Y"], "rxcui": ["1791588", "1791593"], "spl_set_id": ["91e433a9-6800-43a6-ac13-a49a04a5aecd"], "pharm_class_epc": ["Alkylating Drug [EPC]"], "pharm_class_moa": ["Alkylating Activity [MoA]"], "manufacturer_name": ["Baxter Healthcare Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, SINGLE-DOSE in 1 CARTON (10019-926-02)  / 60 mL in 1 VIAL, SINGLE-DOSE (10019-926-16)", "package_ndc": "10019-926-02", "marketing_start_date": "19881230"}], "brand_name": "IFOSFAMIDE", "product_id": "10019-926_7fd51853-2c9b-4291-85a8-a8ebf8782a92", "dosage_form": "INJECTION, POWDER, FOR SOLUTION", "pharm_class": ["Alkylating Activity [MoA]", "Alkylating Drug [EPC]"], "product_ndc": "10019-926", "generic_name": "IFOSFAMIDE", "labeler_name": "Baxter Healthcare Corporation", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "IFOSFAMIDE", "active_ingredients": [{"name": "IFOSFAMIDE", "strength": "3 g/60mL"}], "application_number": "NDA019763", "marketing_category": "NDA", "marketing_start_date": "19881230", "listing_expiration_date": "20261231"}