{
"NDC": {
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"PackageDescription": "2 BOTTLE in 1 CARTON (59726-737-28) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE",
"NDC11Code": "59726-0737-28",
"ProductNDC": "59726-737",
"ProductTypeName": "HUMAN OTC DRUG",
"ProprietaryName": "Omeprazole",
"ProprietaryNameSuffix": null,
"NonProprietaryName": "Omeprazole Magnesium",
"DosageFormName": "TABLET, DELAYED RELEASE",
"RouteName": "ORAL",
"StartMarketingDate": "20200602",
"EndMarketingDate": "20251231",
"MarketingCategoryName": "ANDA",
"ApplicationNumber": "ANDA206582",
"LabelerName": "P & L Development, LLC",
"SubstanceName": "OMEPRAZOLE MAGNESIUM",
"StrengthNumber": "20.6",
"StrengthUnit": "mg/1",
"Pharm_Classes": "Cytochrome P450 2C19 Inhibitors [MoA], Proton Pump Inhibitor [EPC], Proton Pump Inhibitors [MoA]",
"DEASchedule": null,
"Status": "Deprecated",
"LastUpdate": "2026-01-01",
"PackageNdcExcludeFlag": "N",
"ProductNdcExcludeFlag": "N",
"ListingRecordCertifiedThrough": null,
"StartMarketingDatePackage": "20200602",
"EndMarketingDatePackage": "20251231",
"SamplePackage": "N"
}
}