Package 0143-9270-01

Brand: floxuridine

Generic: floxuridine
NDC Package

Package Facts

Identity

Package NDC 0143-9270-01
Digits Only 0143927001
Product NDC 0143-9270
Product ID 0143-9270_0ee8505b-6680-410d-94bf-d55558a8c0e8
Description

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

Marketing

Marketing Status
Marketed Since 2018-02-15
Brand floxuridine
Generic floxuridine
Sample Package No

Linked Drug Pages (1)

Floxuridine ndc-match (0.95)

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"}