NDC 87333-001 – Cardiolite

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

Human Prescription Drug

Product NDC87333-001

Product details

Brand name
Cardiolite
Generic name
Tetrakis(2-methoxyisobutylisocyanide)copper(i) Tetrafluoroborate
Labeler
SHINE SPECT USA, LLC
Dosage form
Injection, Powder, Lyophilized, For Solution
Route
Intravenous
Marketing category
NDA · NDA019785
Marketed since
September 10, 2026
Listing expires
December 31, 2027

Active ingredients

Uses, dosage, side effects and warnings for Cardiolite →

Package NDC codes (2)

Package NDCDescriptionSince
87333-001-2020 VIAL in 1 BOX (87333-001-20) / 5 mL in 1 VIALSep 10, 2026
87333-001-555 VIAL in 1 BOX (87333-001-55) / 5 mL in 1 VIALSep 10, 2026

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