Cupric Chloride 70069-0506-25

Package NDC

70069-0506-25

Manufacturer: Somerset Therapeutics, Llc
Dosage Form: Injection
Route: Intravenous
Product Type: Human Prescription Drug
Marketing Start: May 14, 2024
Listing Expires: December 31, 2026
Application: ANDA216113

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Active Ingredients

Ingredient	Strength
Cupric Chloride	.4 mg/mL

Selected Package

70069-0506-25Selected

25 VIAL, PLASTIC in 1 CARTON (70069-506-25) / 10 mL in 1 VIAL, PLASTIC (70069-506-01)