NDC 72819-234 – Cupric Chloride

Cupric Chloride .4 mg/mL · Injection, Solution · Intravenous

Human Prescription Drug

Product NDC72819-234

Product details

Brand name
Cupric Chloride
Generic name
Cupric Chloride
Labeler
Archis Pharma LLC
Dosage form
Injection, Solution
Route
Intravenous
Marketing category
ANDA · ANDA217626
Marketed since
October 1, 2024
Listing expires
December 31, 2026

Active ingredients

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

Package NDC codes (2)

Package NDCDescriptionSince
72819-234-1625 VIAL, SINGLE-DOSE in 1 PACKAGE (72819-234-16) / 10 mL in 1 VIAL, SINGLE-DOSE (72819-234-06)Jul 5, 2024
72819-234-9925 VIAL, SINGLE-DOSE in 1 PACKAGE (72819-234-99) / 10 mL in 1 VIAL, SINGLE-DOSE (72819-234-96)Oct 1, 2024

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