Package 0078-0734-61

Brand: ilaris

Generic: canakinumab
NDC Package

Package Facts

Identity

Package NDC 0078-0734-61
Digits Only 0078073461
Product NDC 0078-0734
Product ID 0078-0734_45376297-5629-4f69-a583-48a97e905a82
Description

1 VIAL, SINGLE-USE in 1 CARTON (0078-0734-61) / 1 mL in 1 VIAL, SINGLE-USE

Marketing

Marketing Status
Marketed Since 2016-12-22
Brand ilaris
Generic canakinumab
Sample Package No

Linked Drug Pages (1)

Ilaris ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["SUBCUTANEOUS"], "spl_id": "45376297-5629-4f69-a583-48a97e905a82", "openfda": {"unii": ["37CQ2C7X93"], "rxcui": ["1864324", "1864326"], "spl_set_id": ["7d271f3b-e4f9-4d80-8dcf-28d49123f80e"], "manufacturer_name": ["Novartis Pharmaceuticals Corporation"], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, SINGLE-USE in 1 CARTON (0078-0734-61)  / 1 mL in 1 VIAL, SINGLE-USE", "package_ndc": "0078-0734-61", "marketing_start_date": "20161222"}], "brand_name": "Ilaris", "product_id": "0078-0734_45376297-5629-4f69-a583-48a97e905a82", "dosage_form": "INJECTION, SOLUTION", "product_ndc": "0078-0734", "generic_name": "canakinumab", "labeler_name": "Novartis Pharmaceuticals Corporation", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Ilaris", "active_ingredients": [{"name": "CANAKINUMAB", "strength": "150 mg/mL"}], "application_number": "BLA125319", "marketing_category": "BLA", "marketing_start_date": "20161222", "listing_expiration_date": "20261231"}