Package 63323-562-10

{"route": ["INTRAVENOUS"], "spl_id": "2f51e657-4541-4458-8020-5063efc51eb7", "openfda": {"nui": ["N0000175980", "N0000175518", "N0000009963"], "upc": ["0363323562014"], "unii": ["TN9BEX005G"], "rxcui": ["308769"], "spl_set_id": ["af943fa0-ab0f-4b62-9ff0-54ee24cdb772"], "pharm_class_epc": ["Anti-coagulant [EPC]", "Direct Thrombin Inhibitor [EPC]"], "pharm_class_moa": ["Thrombin Inhibitors [MoA]"], "manufacturer_name": ["Fresenius Kabi USA, LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL, SINGLE-USE in 1 CARTON (63323-562-10)  / 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL, SINGLE-USE", "package_ndc": "63323-562-10", "marketing_start_date": "20161028"}], "brand_name": "Bivalirudin", "product_id": "63323-562_2f51e657-4541-4458-8020-5063efc51eb7", "dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION", "pharm_class": ["Anti-coagulant [EPC]", "Direct Thrombin Inhibitor [EPC]", "Thrombin Inhibitors [MoA]"], "product_ndc": "63323-562", "generic_name": "Bivalirudin", "labeler_name": "Fresenius Kabi USA, LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Bivalirudin", "active_ingredients": [{"name": "BIVALIRUDIN", "strength": "250 mg/1"}], "application_number": "ANDA090189", "marketing_category": "ANDA", "marketing_start_date": "20161028", "listing_expiration_date": "20261231"}