{
"NDC": {
"NDCCode": "70518-0165-0",
"PackageDescription": "4 TABLET in 1 BOTTLE (70518-0165-0) ",
"NDC11Code": "70518-0165-00",
"ProductNDC": "70518-0165",
"ProductTypeName": "HUMAN PRESCRIPTION DRUG",
"ProprietaryName": "Promethazine Hydrochloride",
"ProprietaryNameSuffix": null,
"NonProprietaryName": "Promethazine Hydrochloride",
"DosageFormName": "TABLET",
"RouteName": "ORAL",
"StartMarketingDate": "20170120",
"EndMarketingDate": null,
"MarketingCategoryName": "ANDA",
"ApplicationNumber": "ANDA091179",
"LabelerName": "REMEDYREPACK INC.",
"SubstanceName": "PROMETHAZINE HYDROCHLORIDE",
"StrengthNumber": "25",
"StrengthUnit": "mg/1",
"Pharm_Classes": "Phenothiazine [EPC],Phenothiazines [CS]",
"DEASchedule": null,
"Status": "Deprecated",
"LastUpdate": "2019-12-12",
"PackageNdcExcludeFlag": "N",
"ProductNdcExcludeFlag": "N",
"ListingRecordCertifiedThrough": "20201231",
"StartMarketingDatePackage": "20190120",
"EndMarketingDatePackage": null,
"SamplePackage": "N"
}
}