| NDC Code | 51991-642-10 |
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| Package Description | 1000 CAPSULE, DELAYED RELEASE PELLETS in 1 BOTTLE (51991-642-10) |
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| Product NDC | 51991-642 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Omeprazole |
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| Non-Proprietary Name | Omeprazole |
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| Dosage Form | CAPSULE, DELAYED RELEASE PELLETS |
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| Usage | ORAL |
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| Start Marketing Date | 20170703 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA203481 |
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| Manufacturer | Breckenridge Pharmaceutical, Inc. |
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| Substance Name | OMEPRAZOLE |
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| Strength | 10 |
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| Strength Unit | mg/1 |
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| Pharmacy Classes | Proton Pump Inhibitor [EPC],Proton Pump Inhibitors [MoA],Cytochrome P450 2C19 Inhibitors [MoA] |
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