Package 73090-420-01

Brand: sylvant

Generic: siltuximab
NDC Package

Package Facts

Identity

Package NDC 73090-420-01
Digits Only 7309042001
Product NDC 73090-420
Product ID 73090-420_c32bb83e-f9f4-4a6e-928a-f736138996b6
Description

1 VIAL, SINGLE-DOSE in 1 BOX (73090-420-01) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, SINGLE-DOSE

Marketing

Marketing Status
Marketed Since 2014-04-23
Brand sylvant
Generic siltuximab
Sample Package No

Linked Drug Pages (1)

Sylvant ndc-match (0.95)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAVENOUS"], "spl_id": "c32bb83e-f9f4-4a6e-928a-f736138996b6", "openfda": {"nui": ["N0000191006", "N0000191004"], "unii": ["T4H8FMA7IM"], "rxcui": ["1658132", "1658135", "1658139", "1658141"], "spl_set_id": ["8d663642-f52e-49c0-a023-2da083fdfc0b"], "pharm_class_epc": ["Interleukin-6 Antagonist [EPC]"], "pharm_class_moa": ["Interleukin-6 Antagonists [MoA]"], "manufacturer_name": ["Recordati Rare Diseases, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "1 VIAL, SINGLE-DOSE in 1 BOX (73090-420-01)  / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, SINGLE-DOSE", "package_ndc": "73090-420-01", "marketing_start_date": "20140423"}], "brand_name": "Sylvant", "product_id": "73090-420_c32bb83e-f9f4-4a6e-928a-f736138996b6", "dosage_form": "INJECTION, POWDER, FOR SOLUTION", "pharm_class": ["Interleukin-6 Antagonist [EPC]", "Interleukin-6 Antagonists [MoA]"], "product_ndc": "73090-420", "generic_name": "Siltuximab", "labeler_name": "Recordati Rare Diseases, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Sylvant", "active_ingredients": [{"name": "SILTUXIMAB", "strength": "100 mg/1"}], "application_number": "BLA125496", "marketing_category": "BLA", "marketing_start_date": "20140423", "listing_expiration_date": "20261231"}