{
"NDC": {
"NDCCode": "53808-1104-1",
"PackageDescription": "30 TABLET, SUGAR COATED in 1 BLISTER PACK (53808-1104-1) ",
"NDC11Code": "53808-1104-01",
"ProductNDC": "53808-1104",
"ProductTypeName": "HUMAN PRESCRIPTION DRUG",
"ProprietaryName": "Chlorpromazine Hydrochloride",
"ProprietaryNameSuffix": null,
"NonProprietaryName": "Chlorpromazine Hydrochloride",
"DosageFormName": "TABLET, SUGAR COATED",
"RouteName": "ORAL",
"StartMarketingDate": "20180103",
"EndMarketingDate": null,
"MarketingCategoryName": "ANDA",
"ApplicationNumber": "ANDA084113",
"LabelerName": "DOH CENTRAL PHARMACY",
"SubstanceName": "CHLORPROMAZINE HYDROCHLORIDE",
"StrengthNumber": "50",
"StrengthUnit": "mg/1",
"Pharm_Classes": "Phenothiazine [EPC], Phenothiazines [CS]",
"DEASchedule": null,
"Status": "Deprecated",
"LastUpdate": "2024-01-02",
"PackageNdcExcludeFlag": "N",
"ProductNdcExcludeFlag": "N",
"ListingRecordCertifiedThrough": "20231231",
"StartMarketingDatePackage": "20180103",
"EndMarketingDatePackage": null,
"SamplePackage": "N"
}
}