NDC 11994-001 – Cardiolite

Tetrakis(2-methoxyisobutylisocyanide)copper(i) Tetrafluoroborate 1 mg/mL · Injection, Powder, Lyophilized, For Solution · Intravenous

Human Prescription Drug

Product NDC11994-001

Product details

Brand name
Cardiolite
Generic name
Tetrakis(2-methoxyisobutylisocyanide)copper(i) Tetrafluoroborate
Labeler
Lantheus Medical Imaging, Inc.
Dosage form
Injection, Powder, Lyophilized, For Solution
Route
Intravenous
Marketing category
NDA · NDA019785
Marketed since
December 20, 1990
Listing expires
December 31, 2026

Active ingredients

Uses, dosage, side effects and warnings for Cardiolite →

Package NDC codes (2)

Package NDCDescriptionSince
11994-001-2020 VIAL in 1 BOX (11994-001-20) / 5 mL in 1 VIALFeb 28, 2008
11994-001-555 VIAL in 1 BOX (11994-001-55) / 5 mL in 1 VIALDec 20, 1990

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