Package 63323-145-07

Brand: floxuridine

Generic: floxuridine
NDC Package

Package Facts

Identity

Package NDC 63323-145-07
Digits Only 6332314507
Product NDC 63323-145
Product ID 63323-145_a329ca66-d65a-4fd0-a2d9-b8e70ce3bcf8
Description

1 VIAL in 1 CARTON (63323-145-07) / 5 mL in 1 VIAL

Marketing

Marketing Status
Marketed Since 2001-03-15
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": "a329ca66-d65a-4fd0-a2d9-b8e70ce3bcf8", "openfda": {"nui": ["N0000180853", "M0006020"], "unii": ["039LU44I5M"], "rxcui": ["310351"], "spl_set_id": ["c8edabc1-67cd-421b-a147-7c1f19f05b8e"], "pharm_class_cs": ["Deoxyuridine [CS]"], "pharm_class_epc": ["Antimetabolite [EPC]"], "manufacturer_name": ["Fresenius Kabi USA, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL in 1 CARTON (63323-145-07)  / 5 mL in 1 VIAL", "package_ndc": "63323-145-07", "marketing_start_date": "20010315"}], "brand_name": "Floxuridine", "product_id": "63323-145_a329ca66-d65a-4fd0-a2d9-b8e70ce3bcf8", "dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION", "pharm_class": ["Antimetabolite [EPC]", "Deoxyuridine [CS]"], "product_ndc": "63323-145", "generic_name": "FLOXURIDINE", "labeler_name": "Fresenius Kabi USA, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Floxuridine", "active_ingredients": [{"name": "FLOXURIDINE", "strength": "500 mg/5mL"}], "application_number": "ANDA075837", "marketing_category": "ANDA", "marketing_start_date": "20010315", "listing_expiration_date": "20261231"}