{
"NDC": {
"NDCCode": "51655-880-30",
"PackageDescription": "30 TABLET, FILM COATED in 1 BOTTLE (51655-880-30)",
"NDC11Code": "51655-0880-30",
"ProductNDC": "51655-880",
"ProductTypeName": "HUMAN PRESCRIPTION DRUG",
"ProprietaryName": "Atorvastatin Calcium",
"ProprietaryNameSuffix": null,
"NonProprietaryName": "Atorvastatin Calcium",
"DosageFormName": "TABLET, FILM COATED",
"RouteName": "ORAL",
"StartMarketingDate": "20140428",
"EndMarketingDate": null,
"MarketingCategoryName": "ANDA",
"ApplicationNumber": "ANDA020702",
"LabelerName": "Northwind Pharmaceuticals",
"SubstanceName": "ATORVASTATIN CALCIUM",
"StrengthNumber": "80",
"StrengthUnit": "mg/301",
"Pharm_Classes": "HMG-CoA Reductase Inhibitor [EPC],Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]",
"DEASchedule": null,
"Status": "Deprecated",
"LastUpdate": "2019-09-21",
"PackageNdcExcludeFlag": null,
"ProductNdcExcludeFlag": "E",
"ListingRecordCertifiedThrough": "20181231",
"StartMarketingDatePackage": null,
"EndMarketingDatePackage": null,
"SamplePackage": null
}
}