Pantoprazole Sodium 71839-0122
Product NDC
71839-0122- 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]
Packaging Options(3)
1 VIAL in 1 CARTON (71839-122-01) / 10 mL in 1 VIAL
10 CARTON in 1 PACKAGE (71839-122-10) / 1 VIAL in 1 CARTON / 10 mL in 1 VIAL
25 CARTON in 1 PACKAGE (71839-122-25) / 1 VIAL in 1 CARTON / 10 mL in 1 VIAL