Pantoprazole Sodium 70095-0024
Product NDC
70095-0024- Manufacturer
- Sun Pharmaceutical Industries Limited
- Dosage Form
- Injection, Powder, Lyophilized, For Solution
- Route
- Intravenous
- Product Type
- Human Prescription Drug
- Marketing Start
- April 3, 2023
- Listing Expires
- December 31, 2026
- Application
- ANDA204400
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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(2)
10 CARTON in 1 PACKAGE (70095-024-02) / 1 VIAL in 1 CARTON / 10 mL in 1 VIAL (70095-024-01)
25 CARTON in 1 PACKAGE (70095-024-03) / 1 VIAL in 1 CARTON / 10 mL in 1 VIAL (70095-024-01)