"87333-001-55" National Drug Code (NDC)

NDC Code	87333-001-55
Package Description	5 VIAL in 1 BOX (87333-001-55) / 5 mL in 1 VIAL
Product NDC	87333-001
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Cardiolite
Non-Proprietary Name	Tetrakis(2-methoxyisobutylisocyanide)copper(i) Tetrafluoroborate
Dosage Form	INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Usage	INTRAVENOUS
Start Marketing Date	20260910
Marketing Category Name	NDA
Application Number	NDA019785
Manufacturer	SHINE SPECT USA, LLC
Substance Name	TETRAKIS(2-METHOXYISOBUTYLISOCYANIDE)COPPER(I) TETRAFLUOROBORATE
Strength	1
Strength Unit	mg/mL