{
"NDC": {
"NDCCode": "21130-338-06",
"PackageDescription": "177 mL in 1 BOTTLE (21130-338-06) ",
"NDC11Code": "21130-0338-06",
"ProductNDC": "21130-338",
"ProductTypeName": "HUMAN OTC DRUG",
"ProprietaryName": "Dm Max Relief",
"ProprietaryNameSuffix": "Maximum Strength",
"NonProprietaryName": "Dextromethorphan Hydrobromide, Guaifenesin",
"DosageFormName": "LIQUID",
"RouteName": "ORAL",
"StartMarketingDate": "20140731",
"EndMarketingDate": "20201231",
"MarketingCategoryName": "OTC MONOGRAPH FINAL",
"ApplicationNumber": "part341",
"LabelerName": "Safeway, Inc.",
"SubstanceName": "DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN",
"StrengthNumber": "20; 400",
"StrengthUnit": "mg/20mL; mg/20mL",
"Pharm_Classes": null,
"DEASchedule": null,
"Status": "Deprecated",
"LastUpdate": "2021-01-01",
"PackageNdcExcludeFlag": "N",
"ProductNdcExcludeFlag": "N",
"ListingRecordCertifiedThrough": null,
"StartMarketingDatePackage": "20140731",
"EndMarketingDatePackage": "20201231",
"SamplePackage": "N"
}
}