{
"NDC": {
"NDCCode": "68682-990-30",
"PackageDescription": "30 PACKET in 1 CARTON (68682-990-30) / 1 POWDER, FOR SUSPENSION in 1 PACKET",
"NDC11Code": "68682-0990-30",
"ProductNDC": "68682-990",
"ProductTypeName": "HUMAN PRESCRIPTION DRUG",
"ProprietaryName": "Omeprazole And Sodium Bicarbonate",
"ProprietaryNameSuffix": null,
"NonProprietaryName": "Omeprazole, Sodium Bicarbonate",
"DosageFormName": "POWDER, FOR SUSPENSION",
"RouteName": "ORAL",
"StartMarketingDate": "20040615",
"EndMarketingDate": "20260831",
"MarketingCategoryName": "NDA AUTHORIZED GENERIC",
"ApplicationNumber": "NDA021636",
"LabelerName": "Oceanside Pharmaceuticals",
"SubstanceName": "OMEPRAZOLE; SODIUM BICARBONATE",
"StrengthNumber": "20; 1680",
"StrengthUnit": "mg/1; mg/1",
"Pharm_Classes": "Alkalinizing Activity [MoA], Cytochrome P450 2C19 Inhibitors [MoA], Proton Pump Inhibitor [EPC], Proton Pump Inhibitors [MoA]",
"DEASchedule": null,
"Status": "Active",
"LastUpdate": "2025-05-05",
"PackageNdcExcludeFlag": "N",
"ProductNdcExcludeFlag": "N",
"ListingRecordCertifiedThrough": null,
"StartMarketingDatePackage": "20040615",
"EndMarketingDatePackage": "20260831",
"SamplePackage": "N"
}
}