Pantoprazole Sodium 71839-0122-25

Package NDC

71839-0122-25

Manufacturer: Be Pharmaceuticals Inc.
Dosage Form: Injection, Powder, For Solution
Route: Intravenous
Product Type: Human Prescription Drug
Marketing Start: May 25, 2022
Listing Expires: December 31, 2026
Application: ANDA216171

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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

71839-0122-25Selected

25 CARTON in 1 PACKAGE (71839-122-25) / 1 VIAL in 1 CARTON / 10 mL in 1 VIAL

Other packages for this product(2)

71839-0122-01

1 VIAL in 1 CARTON (71839-122-01) / 10 mL in 1 VIAL

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71839-0122-10

10 CARTON in 1 PACKAGE (71839-122-10) / 1 VIAL in 1 CARTON / 10 mL in 1 VIAL

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