| NDC Code | 70095-024-03 |
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| Package Description | 25 CARTON in 1 PACKAGE (70095-024-03) / 1 VIAL in 1 CARTON / 10 mL in 1 VIAL (70095-024-01) |
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| Product NDC | 70095-024 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Pantoprazole Sodium |
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| Non-Proprietary Name | Pantoprazole Sodium |
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| Dosage Form | INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION |
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| Usage | INTRAVENOUS |
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| Start Marketing Date | 20230403 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA204400 |
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| Manufacturer | Sun Pharmaceutical Industries, Inc. |
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| Substance Name | PANTOPRAZOLE SODIUM |
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| Strength | 40 |
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| Strength Unit | mg/10mL |
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| Pharmacy Classes | Proton Pump Inhibitor [EPC], Proton Pump Inhibitors [MoA] |
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