{
"NDC": {
"NDCCode": "0536-4113-06",
"PackageDescription": "50 TABLET in 1 BOTTLE (0536-4113-06) ",
"NDC11Code": "00536-4113-06",
"ProductNDC": "0536-4113",
"ProductTypeName": "HUMAN OTC DRUG",
"ProprietaryName": "Naproxen Sodium",
"ProprietaryNameSuffix": null,
"NonProprietaryName": "Naproxen Sodium",
"DosageFormName": "TABLET",
"RouteName": "ORAL",
"StartMarketingDate": "20091125",
"EndMarketingDate": "20181231",
"MarketingCategoryName": "ANDA",
"ApplicationNumber": "ANDA079096",
"LabelerName": "Rugby Laboratories, Inc.",
"SubstanceName": "NAPROXEN SODIUM",
"StrengthNumber": "220",
"StrengthUnit": "mg/1",
"Pharm_Classes": null,
"DEASchedule": null,
"Status": "Deprecated",
"LastUpdate": "2019-01-01",
"PackageNdcExcludeFlag": "N",
"ProductNdcExcludeFlag": "N",
"ListingRecordCertifiedThrough": null,
"StartMarketingDatePackage": "20091125",
"EndMarketingDatePackage": "20181231",
"SamplePackage": "N"
}
}