cardiolite
Generic: tetrakis(2-methoxyisobutylisocyanide)copper(i) tetrafluoroborate
Labeler: lantheus medical imaging, inc.Drug Facts
Product Profile
Brand Name
cardiolite
Generic Name
tetrakis(2-methoxyisobutylisocyanide)copper(i) tetrafluoroborate
Labeler
lantheus medical imaging, inc.
Dosage Form
INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Routes
Active Ingredients
tetrakis(2-methoxyisobutylisocyanide)copper(i) tetrafluoroborate 1 mg/mL
Manufacturer
Identifiers & Regulatory
Product NDC
11994-001
Product ID
11994-001_d515f49a-8eb4-42f3-a7ee-1634a4804ca5
Product Type
HUMAN PRESCRIPTION DRUG
Marketing Category
NDA
Application Number
NDA019785
Listing Expiration
2026-12-31
Marketing Start
1990-12-20
Normalized Code Variants
Searchable formats for this product NDC code
Digits Only
11994001
Hyphenated Format
11994-001
Supplemental Identifiers
UNII
Packaging Origin
Original Packager
Resolved Product View
Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.
Resolved Identity
Brand Name
cardiolite (source: ndc)
Generic Name
tetrakis(2-methoxyisobutylisocyanide)copper(i) tetrafluoroborate (source: ndc)
Application Number
NDA019785 (source: ndc)
Routes
source: ndc
Resolved Composition
Strengths
- 1 mg/mL
Packaging
- 20 VIAL in 1 BOX (11994-001-20) / 5 mL in 1 VIAL
- 5 VIAL in 1 BOX (11994-001-55) / 5 mL in 1 VIAL
Packages (2)
Ingredients (1)
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"}