cardiolite

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

Labeler: lantheus medical imaging, inc.
NDC Directory HUMAN PRESCRIPTION DRUG NDA Inactive Finished

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
INTRAVENOUS
Active Ingredients

tetrakis(2-methoxyisobutylisocyanide)copper(i) tetrafluoroborate 1 mg/mL

Manufacturer
Lantheus Medical Imaging, Inc.

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
N6OU7HJ70P

Packaging Origin

Original Packager
true

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
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 1 mg/mL
source: ndc
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
source: ndc

Packages (2)

Ingredients (1)

tetrakis(2-methoxyisobutylisocyanide)copper(i) tetrafluoroborate (1 mg/mL)

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"}