| NDC Code | 68462-390-10 |
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| Package Description | 1000 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE, PLASTIC (68462-390-10) |
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| Product NDC | 68462-390 |
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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 PELLETS |
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| Usage | ORAL |
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| Start Marketing Date | 20211101 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA209495 |
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| Manufacturer | Glenmark Pharmaceuticals Inc., USA |
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| Substance Name | ESOMEPRAZOLE MAGNESIUM |
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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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