{
"NDC": {
"NDCCode": "50844-733-01",
"PackageDescription": "1 BOTTLE in 1 CARTON (50844-733-01) > 30 TABLET, FILM COATED in 1 BOTTLE",
"NDC11Code": "50844-0733-01",
"ProductNDC": "50844-733",
"ProductTypeName": "HUMAN OTC DRUG",
"ProprietaryName": "Mucus Relief Cough",
"ProprietaryNameSuffix": null,
"NonProprietaryName": "Dextromethorphan Hbr And Guaifenesin",
"DosageFormName": "TABLET, FILM COATED",
"RouteName": "ORAL",
"StartMarketingDate": "20051231",
"EndMarketingDate": "20220626",
"MarketingCategoryName": "OTC MONOGRAPH FINAL",
"ApplicationNumber": "part341",
"LabelerName": "L.N.K. International, Inc.",
"SubstanceName": "DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN",
"StrengthNumber": "20; 400",
"StrengthUnit": "mg/1; mg/1",
"Pharm_Classes": "Sigma-1 Agonist [EPC], Sigma-1 Receptor Agonists [MoA], Uncompetitive N-methyl-D-aspartate Receptor Antagonist [EPC], Uncompetitive NMDA Receptor Antagonists [MoA]",
"DEASchedule": null,
"Status": "Deprecated",
"LastUpdate": "2022-06-28",
"PackageNdcExcludeFlag": "N",
"ProductNdcExcludeFlag": "N",
"ListingRecordCertifiedThrough": null,
"StartMarketingDatePackage": "20051231",
"EndMarketingDatePackage": "20220626",
"SamplePackage": "N"
}
}