Pantoprazole Sodium 65219-0385-10

Package NDC

65219-0385-10

Manufacturer: Fresenius Kabi Usa, Llc
Dosage Form: Injection, Powder, Lyophilized, For Solution
Route: Intravenous
Product Type: Human Prescription Drug
Marketing Start: August 1, 2024
Listing Expires: December 31, 2026
Application: ANDA216021

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Active Ingredients

Ingredient	Strength
Pantoprazole Sodium	40 mg/10mL

Drug Class

Proton Pump Inhibitor [EPC]Proton Pump Inhibitors [MoA]

Selected Package

65219-0385-10Selected

10 VIAL in 1 CARTON (65219-385-10) / 10 mL in 1 VIAL (65219-385-01)