| NDC Code | 55150-202-10 |
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| Package Description | 10 VIAL, SINGLE-DOSE in 1 CARTON (55150-202-10) / 1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL, SINGLE-DOSE (55150-202-00) |
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| Product NDC | 55150-202 |
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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, FOR SOLUTION |
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| Usage | INTRAVENOUS |
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| Start Marketing Date | 20160330 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA205675 |
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| Manufacturer | Eugia US LLC |
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| Substance Name | PANTOPRAZOLE SODIUM |
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| Strength | 40 |
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| Strength Unit | mg/1 |
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| Pharmacy Classes | Proton Pump Inhibitor [EPC], Proton Pump Inhibitors [MoA] |
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