| NDC Code | 70436-190-82 |
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| Package Description | 10 VIAL in 1 CARTON (70436-190-82) / 5 mL in 1 VIAL (70436-190-80) |
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| Product NDC | 70436-190 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Esomeprazole Sodium |
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| Non-Proprietary Name | Esomeprazole 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 | 20220225 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA215732 |
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| Manufacturer | Slate Run Pharmaceuticals, LLC |
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| Substance Name | ESOMEPRAZOLE SODIUM |
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| Strength | 40 |
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| Strength Unit | mg/5mL |
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| Pharmacy Classes | Cytochrome P450 2C19 Inhibitors [MoA], Proton Pump Inhibitor [EPC], Proton Pump Inhibitors [MoA] |
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