NDC 70069-506 – Cupric Chloride

Cupric Chloride .4 mg/mL · Injection · Intravenous

Human Prescription Drug

Product NDC70069-506

Product details

Brand name
Cupric Chloride
Generic name
Cupric Chloride
Labeler
Somerset Therapeutics, LLC
Dosage form
Injection
Route
Intravenous
Marketing category
ANDA · ANDA216113
Marketed since
May 14, 2024
Listing expires
December 31, 2027

Active ingredients

Uses, dosage, side effects and warnings for Cupric Chloride →

Package NDC codes (1)

Package NDCDescriptionSince
70069-506-2525 VIAL, PLASTIC in 1 CARTON (70069-506-25) / 10 mL in 1 VIAL, PLASTIC (70069-506-01)May 14, 2024

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