Package 50242-927-01

Brand: hemlibra

Generic: emicizumab
NDC Package

Package Facts

Identity

Package NDC 50242-927-01
Digits Only 5024292701
Product NDC 50242-927
Product ID 50242-927_8f25ff10-e9d1-46a1-9889-e2c3f6e0d432
Description

1 VIAL, SINGLE-USE in 1 CARTON (50242-927-01) / .4 mL in 1 VIAL, SINGLE-USE

Marketing

Marketing Status
Marketed Since 2024-01-31
Brand hemlibra
Generic emicizumab
Sample Package No

Linked Drug Pages (1)

Hemlibra ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["SUBCUTANEOUS"], "spl_id": "8f25ff10-e9d1-46a1-9889-e2c3f6e0d432", "openfda": {"unii": ["7NL2E3F6K3"], "rxcui": ["1989799", "1989804", "1989809", "1989811", "1989814", "1989815", "1989816", "1989817", "2632728", "2632729", "2675567", "2675568"], "spl_set_id": ["2483adba-fab6-4d1b-96c5-c195577ed071"], "manufacturer_name": ["Genentech, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, SINGLE-USE in 1 CARTON (50242-927-01)  / .4 mL in 1 VIAL, SINGLE-USE", "package_ndc": "50242-927-01", "marketing_start_date": "20240131"}], "brand_name": "Hemlibra", "product_id": "50242-927_8f25ff10-e9d1-46a1-9889-e2c3f6e0d432", "dosage_form": "INJECTION, SOLUTION", "product_ndc": "50242-927", "generic_name": "emicizumab", "labeler_name": "Genentech, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Hemlibra", "active_ingredients": [{"name": "EMICIZUMAB", "strength": "12 mg/.4mL"}], "application_number": "BLA761083", "marketing_category": "BLA", "marketing_start_date": "20240131", "listing_expiration_date": "20261231"}