| NDC Code | 0378-2086-77 |
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| Package Description | 90 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE, PLASTIC (0378-2086-77) |
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| Product NDC | 0378-2086 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Dexlansoprazole |
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| Non-Proprietary Name | Dexlansoprazole |
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| Dosage Form | CAPSULE, DELAYED RELEASE PELLETS |
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| Usage | ORAL |
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| Start Marketing Date | 20240122 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA205205 |
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| Manufacturer | Mylan Pharmaceuticals Inc. |
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| Substance Name | DEXLANSOPRAZOLE SESQUIHYDRATE |
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| Strength | 60 |
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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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