| NDC Code | 37808-732-03 |
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| Package Description | 3 BOTTLE in 1 CARTON (37808-732-03) > 14 CAPSULE, GELATIN COATED in 1 BOTTLE |
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| Product NDC | 37808-732 |
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| Product Type Name | HUMAN OTC DRUG |
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| Proprietary Name | Omeprazole And Sodium Bicarbonate |
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| Non-Proprietary Name | Omeprazole, Sodium Bicarbonate |
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| Dosage Form | CAPSULE, GELATIN COATED |
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| Usage | ORAL |
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| Start Marketing Date | 20170825 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA201361 |
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| Manufacturer | H E B |
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| Substance Name | OMEPRAZOLE; SODIUM BICARBONATE |
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| Strength | 20; 1100 |
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| Strength Unit | mg/1; mg/1 |
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| Pharmacy Classes | Cytochrome P450 2C19 Inhibitors [MoA], Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Osmotic Activity [MoA], Osmotic Laxative [EPC], Proton Pump Inhibitor [EPC], Proton Pump Inhibitors [MoA] |
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