{
"NDC": {
"NDCCode": "43602-602-30",
"PackageDescription": "1 BOTTLE in 1 CARTON (43602-602-30) > 30 TABLET in 1 BOTTLE",
"NDC11Code": "43602-0602-30",
"ProductNDC": "43602-602",
"ProductTypeName": "HUMAN OTC DRUG",
"ProprietaryName": "Famotidine",
"ProprietaryNameSuffix": null,
"NonProprietaryName": "Famotidine",
"DosageFormName": "TABLET",
"RouteName": "ORAL",
"StartMarketingDate": "20211103",
"EndMarketingDate": null,
"MarketingCategoryName": "ANDA",
"ApplicationNumber": "ANDA216030",
"LabelerName": "Ascent Pharmaceuticals, Inc.",
"SubstanceName": "FAMOTIDINE",
"StrengthNumber": "20",
"StrengthUnit": "mg/1",
"Pharm_Classes": "Histamine H2 Receptor Antagonists [MoA], Histamine-2 Receptor Antagonist [EPC]",
"DEASchedule": null,
"Status": "Active",
"LastUpdate": "2022-02-19",
"PackageNdcExcludeFlag": "N",
"ProductNdcExcludeFlag": "N",
"ListingRecordCertifiedThrough": "20261231",
"StartMarketingDatePackage": "20211103",
"EndMarketingDatePackage": null,
"SamplePackage": "N"
}
}