🇺🇸
United States · US · US:63323-145_a329ca66-d65a-4fd0-a2d9-b8e70ce3bcf8
Floxuridine
Orange BookUNIISPLATC L01BC09
Last synced from FDA National Drug Code directory (United States) on
Identification
ManufacturerFresenius Kabi USA, LLC
CountryUS (United States)
ATC codeL01BC09
Dispensing—
ReimbursedNo
SourceFDA National Drug Code directory (United States)
Last synced6/3/2026
Packs · 1
- ndc1163323145071 VIAL in 1 CARTON (63323-145-07) / 5 mL in 1 VIAL
Annotations
UNII (FDA Substance ID)
039LU44I5M
FLOXURIDINE
RxCUI 4488
Orange Book
A075837
AP
DailyMed SPL labels
1 version tracked
Raw payload (JSON)
{
"unii": {
"unii": "039LU44I5M",
"rxcui": "4488",
"inchikey": "ODKNJVUHOIMIIZ-RRKCRQDMSA-N",
"display_name": "FLOXURIDINE",
"substance_type": "chemical",
"ingredient_type": "INGREDIENT SUBSTANCE"
},
"route": "INTRA-ARTERIAL",
"spl_meta": {
"c8edabc1-67cd-421b-a147-7c1f19f05b8e": {
"match": "brand_token",
"title": "FLOXURIDINE (FLOXURIDINE) INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION [FRESENIUS KABI USA, LLC]",
"spl_version": "4",
"published_date": "2024-10-21"
}
},
"productid": "63323-145_a329ca66-d65a-4fd0-a2d9-b8e70ce3bcf8",
"productndc": "63323-145",
"dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION",
"orange_book": {
"appl_no": "075837",
"products": [
{
"rs": false,
"rld": false,
"te_code": "AP",
"strength": "500MG/VIAL",
"product_no": "001",
"approval_date": "Feb 22, 2001"
}
],
"appl_type": "A"
},
"dea_schedule": null,
"product_type": "HUMAN PRESCRIPTION DRUG",
"substance_name": "FLOXURIDINE",
"proprietary_name": "Floxuridine",
"active_ingred_unit": "mg/5mL",
"application_number": "ANDA075837",
"marketing_category": "ANDA",
"nonproprietary_name": "FLOXURIDINE",
"start_marketing_date": "20010315",
"active_numerator_strength": "500"
}Related drugs
Other records sharing ATC code L01BC09.
Access this data programmatically
Query Floxuridine and 610,000+ other drug records through a single REST API — with a last_synced_at provenance stamp on every response. Free tier includes 100 requests/day.