| NDC Code | 72789-352-30 |
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| Package Description | 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE, PLASTIC (72789-352-30) |
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| Product NDC | 72789-352 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Esomeprazole Magnesium |
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| Non-Proprietary Name | Esomeprazole Magnesium |
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| Dosage Form | CAPSULE, DELAYED RELEASE |
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| Usage | ORAL |
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| Start Marketing Date | 20160421 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA205606 |
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| Manufacturer | PD-Rx Pharmaceuticals, Inc. |
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| Substance Name | ESOMEPRAZOLE MAGNESIUM DIHYDRATE |
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| Strength | 20 |
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| Strength Unit | mg/1 |
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| Pharmacy Classes | Cytochrome P450 2C19 Inhibitors [MoA], Proton Pump Inhibitor [EPC], Proton Pump Inhibitors [MoA] |
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