| NDC Code | 49884-269-11 |
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| Package Description | 30 PACKET in 1 CARTON (49884-269-11) / 1 POWDER, FOR SUSPENSION in 1 PACKET (49884-269-52) |
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| Product NDC | 49884-269 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Omeprazole/sodium Bicarbonate |
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| Non-Proprietary Name | Omeprazole And Sodium Bicarbonate |
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| Dosage Form | POWDER, FOR SUSPENSION |
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| Usage | ORAL |
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| Start Marketing Date | 20160718 |
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| End Marketing Date | 20241130 |
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| Marketing Category Name | ANDA |
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| Application Number | ANDA079182 |
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| Manufacturer | Par Pharmaceutical, Inc. |
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| Substance Name | OMEPRAZOLE; SODIUM BICARBONATE |
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| Strength | 40; 1680 |
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| Strength Unit | mg/1; mg/1 |
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| Pharmacy Classes | Alkalinizing Activity [MoA], Cytochrome P450 2C19 Inhibitors [MoA], Proton Pump Inhibitor [EPC], Proton Pump Inhibitors [MoA] |
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