{
"NDC": {
"NDCCode": "70518-0033-0",
"PackageDescription": "12 TABLET in 1 BLISTER PACK (70518-0033-0) ",
"NDC11Code": "70518-0033-00",
"ProductNDC": "70518-0033",
"ProductTypeName": "HUMAN PRESCRIPTION DRUG",
"ProprietaryName": "Alendronate Sodium",
"ProprietaryNameSuffix": null,
"NonProprietaryName": "Alendronate Sodium",
"DosageFormName": "TABLET",
"RouteName": "ORAL",
"StartMarketingDate": "20161201",
"EndMarketingDate": null,
"MarketingCategoryName": "ANDA",
"ApplicationNumber": "ANDA076768",
"LabelerName": "REMEDYREPACK INC.",
"SubstanceName": "ALENDRONATE SODIUM",
"StrengthNumber": "70",
"StrengthUnit": "mg/1",
"Pharm_Classes": "Bisphosphonate [EPC], Diphosphonates [CS]",
"DEASchedule": null,
"Status": "Active",
"LastUpdate": "2026-01-08",
"PackageNdcExcludeFlag": "N",
"ProductNdcExcludeFlag": "N",
"ListingRecordCertifiedThrough": "20271231",
"StartMarketingDatePackage": "20161201",
"EndMarketingDatePackage": null,
"SamplePackage": "N"
}
}