floxuridine

Generic: floxuridine

Labeler: hikma pharmaceuticals usa inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name floxuridine
Generic Name floxuridine
Labeler hikma pharmaceuticals usa inc.
Dosage Form INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Routes
INTRA-ARTERIAL
Active Ingredients

floxuridine 100 mg/mL

Manufacturer
Hikma Pharmaceuticals USA Inc.

Identifiers & Regulatory

Product NDC 0143-9270
Product ID 0143-9270_0ee8505b-6680-410d-94bf-d55558a8c0e8
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number ANDA075387
Listing Expiration 2026-12-31
Marketing Start 2018-02-15

Pharmacologic Class

Established (EPC)
antimetabolite [epc]
Chemical Structure
deoxyuridine [cs]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 01439270
Hyphenated Format 0143-9270

Supplemental Identifiers

RxCUI
310351
UNII
039LU44I5M
NUI
N0000180853 M0006020

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 floxuridine (source: ndc)
Generic Name floxuridine (source: ndc)
Application Number ANDA075387 (source: ndc)
Routes
INTRA-ARTERIAL
source: ndc

Resolved Composition

Strengths
  • 100 mg/mL
source: ndc
Packaging
  • 1 VIAL in 1 BOX, UNIT-DOSE (0143-9270-01) / 5 mL in 1 VIAL
source: ndc

Packages (1)

0143-9270-01 1 VIAL in 1 BOX, UNIT-DOSE (0143-9270-01) / 5 mL in 1 VIAL

Ingredients (1)

floxuridine (100 mg/mL)

Linked Drug Pages (1)

Floxuridine ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRA-ARTERIAL"], "spl_id": "0ee8505b-6680-410d-94bf-d55558a8c0e8", "openfda": {"nui": ["N0000180853", "M0006020"], "unii": ["039LU44I5M"], "rxcui": ["310351"], "spl_set_id": ["e3c2e3e7-bc83-465d-b615-3ad56580b3a7"], "pharm_class_cs": ["Deoxyuridine [CS]"], "pharm_class_epc": ["Antimetabolite [EPC]"], "manufacturer_name": ["Hikma Pharmaceuticals USA Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL in 1 BOX, UNIT-DOSE (0143-9270-01)  / 5 mL in 1 VIAL", "package_ndc": "0143-9270-01", "marketing_start_date": "20180215"}], "brand_name": "Floxuridine", "product_id": "0143-9270_0ee8505b-6680-410d-94bf-d55558a8c0e8", "dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION", "pharm_class": ["Antimetabolite [EPC]", "Deoxyuridine [CS]"], "product_ndc": "0143-9270", "generic_name": "Floxuridine", "labeler_name": "Hikma Pharmaceuticals USA Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Floxuridine", "active_ingredients": [{"name": "FLOXURIDINE", "strength": "100 mg/mL"}], "application_number": "ANDA075387", "marketing_category": "ANDA", "marketing_start_date": "20180215", "listing_expiration_date": "20261231"}