Zinc Sulfate 70069-0692-25

Package NDC

70069-0692-25

Manufacturer: Somerset Therapeutics, Llc
Dosage Form: Solution
Route: Intravenous
Product Type: Human Prescription Drug
Marketing Start: July 18, 2024
Listing Expires: December 31, 2026
Application: ANDA216135

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Active Ingredients

Ingredient	Strength
Zinc Sulfate	3 mg/mL

Drug Class

Copper Absorption Inhibitor [EPC]Decreased Copper Ion Absorption [PE]

Selected Package

70069-0692-25Selected

25 VIAL in 1 CARTON (70069-692-25) / 10 mL in 1 VIAL (70069-692-01)