Cupric Chloride 72603-0351-25

Package NDC

72603-0351-25

Manufacturer: Northstar Rx Llc
Dosage Form: Injection, Solution
Route: Intravenous
Product Type: Human Prescription Drug
Marketing Start: October 1, 2024
Listing Expires: December 31, 2026
Application: ANDA217626

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Active Ingredients

Ingredient	Strength
Cupric Chloride	.4 mg/mL

Selected Package

72603-0351-25Selected

25 VIAL, SINGLE-DOSE in 1 PACKAGE (72603-351-25) / 10 mL in 1 VIAL, SINGLE-DOSE (72603-351-01)