Package 81643-9270-1

{"route": ["INTRA-ARTERIAL"], "spl_id": "42039e70-fc10-450f-9dec-2b0402160bda", "openfda": {"nui": ["N0000180853", "M0006020"], "unii": ["039LU44I5M"], "rxcui": ["310351"], "spl_set_id": ["4681f23e-6b5e-433b-b245-3d0b4e64ebb2"], "pharm_class_cs": ["Deoxyuridine [CS]"], "pharm_class_epc": ["Antimetabolite [EPC]"], "manufacturer_name": ["JND Therapeutics, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL in 1 BOX, UNIT-DOSE (81643-9270-1)  / 5 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL", "package_ndc": "81643-9270-1", "marketing_start_date": "20220609"}], "brand_name": "Floxuridine", "product_id": "81643-9270_42039e70-fc10-450f-9dec-2b0402160bda", "dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION", "pharm_class": ["Antimetabolite [EPC]", "Deoxyuridine [CS]"], "product_ndc": "81643-9270", "generic_name": "Floxuridine", "labeler_name": "JND Therapeutics, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Floxuridine", "active_ingredients": [{"name": "FLOXURIDINE", "strength": "500 mg/1"}], "application_number": "ANDA075387", "marketing_category": "ANDA", "marketing_start_date": "20220609", "listing_expiration_date": "20261231"}