Package 11994-001-20

Brand: cardiolite

Generic: tetrakis(2-methoxyisobutylisocyanide)copper(i) tetrafluoroborate
NDC Package

Package Facts

Identity

Package NDC 11994-001-20
Digits Only 1199400120
Product NDC 11994-001
Description

20 VIAL in 1 BOX (11994-001-20) / 5 mL in 1 VIAL

Marketing

Marketing Status
Marketed Since 2008-02-28
Brand cardiolite
Generic tetrakis(2-methoxyisobutylisocyanide)copper(i) tetrafluoroborate
Sample Package No

Linked Drug Pages (1)

Raw FDA Data

View complete raw FDA NDC JSON payload
{"route": ["INTRAVENOUS"], "spl_id": "d515f49a-8eb4-42f3-a7ee-1634a4804ca5", "openfda": {"unii": ["N6OU7HJ70P"], "spl_set_id": ["49662def-2fb9-47b2-8467-ca56f6006167"], "manufacturer_name": ["Lantheus Medical Imaging, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "20 VIAL in 1 BOX (11994-001-20)  / 5 mL in 1 VIAL", "package_ndc": "11994-001-20", "marketing_start_date": "20080228"}, {"sample": false, "description": "5 VIAL in 1 BOX (11994-001-55)  / 5 mL in 1 VIAL", "package_ndc": "11994-001-55", "marketing_start_date": "19901220"}], "brand_name": "Cardiolite", "product_id": "11994-001_d515f49a-8eb4-42f3-a7ee-1634a4804ca5", "dosage_form": "INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION", "product_ndc": "11994-001", "generic_name": "TETRAKIS(2-METHOXYISOBUTYLISOCYANIDE)COPPER(I) TETRAFLUOROBORATE", "labeler_name": "Lantheus Medical Imaging, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Cardiolite", "active_ingredients": [{"name": "TETRAKIS(2-METHOXYISOBUTYLISOCYANIDE)COPPER(I) TETRAFLUOROBORATE", "strength": "1 mg/mL"}], "application_number": "NDA019785", "marketing_category": "NDA", "marketing_start_date": "19901220", "listing_expiration_date": "20261231"}