{
"NDC": {
"NDCCode": "0378-3569-99",
"PackageDescription": "4 TABLET in 1 BOTTLE, PLASTIC (0378-3569-99) ",
"NDC11Code": "00378-3569-99",
"ProductNDC": "0378-3569",
"ProductTypeName": "HUMAN PRESCRIPTION DRUG",
"ProprietaryName": "Alendronate Sodium",
"ProprietaryNameSuffix": null,
"NonProprietaryName": "Alendronate Sodium",
"DosageFormName": "TABLET",
"RouteName": "ORAL",
"StartMarketingDate": "20110325",
"EndMarketingDate": "20180331",
"MarketingCategoryName": "ANDA",
"ApplicationNumber": "ANDA076584",
"LabelerName": "Mylan Pharmaceuticals Inc.",
"SubstanceName": "ALENDRONATE SODIUM",
"StrengthNumber": "70",
"StrengthUnit": "mg/1",
"Pharm_Classes": "Bisphosphonate [EPC],Diphosphonates [Chemical/Ingredient]",
"DEASchedule": null,
"Status": "Deprecated",
"LastUpdate": "2018-04-03",
"PackageNdcExcludeFlag": "N",
"ProductNdcExcludeFlag": "N",
"ListingRecordCertifiedThrough": "20181231",
"StartMarketingDatePackage": null,
"EndMarketingDatePackage": null,
"SamplePackage": null
}
}