Package 25682-001-01

Brand: soliris

Generic: eculizumab
NDC Package

Package Facts

Identity

Package NDC 25682-001-01
Digits Only 2568200101
Product NDC 25682-001
Product ID 25682-001_25021c88-95e1-42f0-b895-921526b90642
Description

1 VIAL in 1 CARTON (25682-001-01) / 30 mL in 1 VIAL

Marketing

Marketing Status
Marketed Since 2007-04-02
Brand soliris
Generic eculizumab
Sample Package No

Linked Drug Pages (1)

STRENSIQ ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAVENOUS"], "spl_id": "25021c88-95e1-42f0-b895-921526b90642", "openfda": {"nui": ["N0000175575", "N0000175974"], "unii": ["A3ULP0F556"], "rxcui": ["700384", "700387"], "spl_set_id": ["ebcd67fa-b4d1-4a22-b33d-ee8bf6b9c722"], "pharm_class_epc": ["Complement Inhibitor [EPC]"], "pharm_class_moa": ["Complement Inhibitors [MoA]"], "manufacturer_name": ["Alexion Pharmaceuticals Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL in 1 CARTON (25682-001-01)  / 30 mL in 1 VIAL", "package_ndc": "25682-001-01", "marketing_start_date": "20070402"}], "brand_name": "SOLIRIS", "product_id": "25682-001_25021c88-95e1-42f0-b895-921526b90642", "dosage_form": "INJECTION, SOLUTION, CONCENTRATE", "pharm_class": ["Complement Inhibitor [EPC]", "Complement Inhibitors [MoA]"], "product_ndc": "25682-001", "generic_name": "ECULIZUMAB", "labeler_name": "Alexion Pharmaceuticals Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "SOLIRIS", "active_ingredients": [{"name": "ECULIZUMAB", "strength": "300 mg/30mL"}], "application_number": "BLA125166", "marketing_category": "BLA", "marketing_start_date": "20070402", "listing_expiration_date": "20261231"}