{
"NDC": {
"NDCCode": "69367-199-01",
"PackageDescription": "100 TABLET in 1 BOTTLE, PLASTIC (69367-199-01) ",
"NDC11Code": "69367-0199-01",
"ProductNDC": "69367-199",
"ProductTypeName": "HUMAN OTC DRUG",
"ProprietaryName": "Doxylamine Succinate And Phenylephrine Hydrochloride",
"ProprietaryNameSuffix": null,
"NonProprietaryName": "Doxylamine Succinate And Phenylephrine Hydrochloride",
"DosageFormName": "TABLET",
"RouteName": "ORAL",
"StartMarketingDate": "20181025",
"EndMarketingDate": "20240501",
"MarketingCategoryName": "OTC MONOGRAPH FINAL",
"ApplicationNumber": "part341",
"LabelerName": "Westminster Pharmaceuticals, LLC",
"SubstanceName": "DOXYLAMINE SUCCINATE; PHENYLEPHRINE HYDROCHLORIDE",
"StrengthNumber": "7.5; 10",
"StrengthUnit": "mg/1; mg/1",
"Pharm_Classes": "Adrenergic alpha1-Agonists [MoA], Antihistamine [EPC], Histamine Receptor Antagonists [MoA], alpha-1 Adrenergic Agonist [EPC]",
"DEASchedule": null,
"Status": "Deprecated",
"LastUpdate": "2024-05-02",
"PackageNdcExcludeFlag": "N",
"ProductNdcExcludeFlag": "N",
"ListingRecordCertifiedThrough": null,
"StartMarketingDatePackage": "20181025",
"EndMarketingDatePackage": "20240501",
"SamplePackage": "N"
}
}