Package 72572-035-10

{"route": ["INTRAVENOUS"], "spl_id": "53431803-dc0b-42dc-8766-e17c3dbdf4ea", "openfda": {"nui": ["N0000175980", "N0000175518", "N0000009963"], "unii": ["TN9BEX005G"], "rxcui": ["308769"], "spl_set_id": ["19a4afc5-151d-4d3c-bfef-48aa8797d695"], "pharm_class_epc": ["Anti-coagulant [EPC]", "Direct Thrombin Inhibitor [EPC]"], "pharm_class_moa": ["Thrombin Inhibitors [MoA]"], "manufacturer_name": ["Civica, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL, SINGLE-USE in 1 CARTON (72572-035-10)  / 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL, SINGLE-USE (72572-035-01)", "package_ndc": "72572-035-10", "marketing_start_date": "20201221"}], "brand_name": "bivalirudin", "product_id": "72572-035_53431803-dc0b-42dc-8766-e17c3dbdf4ea", "dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION", "pharm_class": ["Anti-coagulant [EPC]", "Direct Thrombin Inhibitor [EPC]", "Thrombin Inhibitors [MoA]"], "product_ndc": "72572-035", "generic_name": "bivalirudin", "labeler_name": "Civica, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "bivalirudin", "active_ingredients": [{"name": "BIVALIRUDIN", "strength": "250 mg/1"}], "application_number": "NDA020873", "marketing_category": "NDA AUTHORIZED GENERIC", "marketing_start_date": "20201221", "listing_expiration_date": "20261231"}