| NDC Code | 47335-509-44 |
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| Package Description | 10 VIAL, SINGLE-USE in 1 CARTON (47335-509-44) > 5 mL in 1 VIAL, SINGLE-USE (47335-509-40) |
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| Product NDC | 47335-509 |
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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 | 20140103 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA200882 |
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| Manufacturer | Sun Pharma Global FZE |
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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 | Proton Pump Inhibitor [EPC],Proton Pump Inhibitors [MoA],Cytochrome P450 2C19 Inhibitors [MoA] |
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