{
"NDC": {
"NDCCode": "50580-506-25",
"PackageDescription": "1 BOTTLE in 1 CARTON (50580-506-25) > 225 TABLET, FILM COATED in 1 BOTTLE",
"NDC11Code": "50580-0506-25",
"ProductNDC": "50580-506",
"ProductTypeName": "HUMAN OTC DRUG",
"ProprietaryName": "Tylenol Pm",
"ProprietaryNameSuffix": "Extra Strength",
"NonProprietaryName": "Acetaminophen And Diphenhydramine Hydrochloride",
"DosageFormName": "TABLET, FILM COATED",
"RouteName": "ORAL",
"StartMarketingDate": "20140929",
"EndMarketingDate": null,
"MarketingCategoryName": "OTC MONOGRAPH NOT FINAL",
"ApplicationNumber": "part343",
"LabelerName": "Johnson & Johnson Consumer Inc., McNeil Consumer Healthcare Division",
"SubstanceName": "ACETAMINOPHEN; DIPHENHYDRAMINE HYDROCHLORIDE",
"StrengthNumber": "500; 25",
"StrengthUnit": "mg/1; mg/1",
"Pharm_Classes": null,
"DEASchedule": null,
"Status": "Deprecated",
"LastUpdate": "2018-09-28",
"PackageNdcExcludeFlag": "N",
"ProductNdcExcludeFlag": "N",
"ListingRecordCertifiedThrough": "20181231",
"StartMarketingDatePackage": "20140929",
"EndMarketingDatePackage": null,
"SamplePackage": "N"
}
}