Package 55150-210-10
Brand: bivalirudin
Generic: bivalirudinPackage Facts
Identity
Package NDC
55150-210-10
Digits Only
5515021010
Product NDC
55150-210
Description
10 VIAL, SINGLE-DOSE in 1 CARTON (55150-210-10) / 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL, SINGLE-DOSE
Marketing
Marketing Status
Brand
bivalirudin
Generic
bivalirudin
Sample Package
No
Linked Drug Pages (1)
Raw FDA Data
View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "eb82831b-a234-4818-bbf2-e75e45647b77", "openfda": {"nui": ["N0000175980", "N0000175518", "N0000009963"], "upc": ["0355150210107"], "unii": ["TN9BEX005G"], "rxcui": ["308769"], "spl_set_id": ["e574d04f-67b4-4a84-9d66-8c2d54f95120"], "pharm_class_epc": ["Anti-coagulant [EPC]", "Direct Thrombin Inhibitor [EPC]"], "pharm_class_moa": ["Thrombin Inhibitors [MoA]"], "manufacturer_name": ["Eugia US LLC"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "10 VIAL, SINGLE-DOSE in 1 CARTON (55150-210-10) / 1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 VIAL, SINGLE-DOSE", "package_ndc": "55150-210-10", "marketing_start_date": "20180727"}], "brand_name": "BIVALIRUDIN", "product_id": "55150-210_eb82831b-a234-4818-bbf2-e75e45647b77", "dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION", "pharm_class": ["Anti-coagulant [EPC]", "Direct Thrombin Inhibitor [EPC]", "Thrombin Inhibitors [MoA]"], "product_ndc": "55150-210", "generic_name": "BIVALIRUDIN", "labeler_name": "Eugia US LLC", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "BIVALIRUDIN", "active_ingredients": [{"name": "BIVALIRUDIN", "strength": "250 mg/1"}], "application_number": "ANDA205962", "marketing_category": "ANDA", "marketing_start_date": "20180727", "listing_expiration_date": "20261231"}