{
"NDC": {
"NDCCode": "61919-303-30",
"PackageDescription": "30 TABLET, FILM COATED in 1 BOTTLE (61919-303-30) ",
"NDC11Code": "61919-0303-30",
"ProductNDC": "61919-303",
"ProductTypeName": "HUMAN PRESCRIPTION DRUG",
"ProprietaryName": "Atorvastatin Calcium",
"ProprietaryNameSuffix": null,
"NonProprietaryName": "Atorvastatin",
"DosageFormName": "TABLET, FILM COATED",
"RouteName": "ORAL",
"StartMarketingDate": "20180314",
"EndMarketingDate": null,
"MarketingCategoryName": "ANDA",
"ApplicationNumber": "ANDA090548",
"LabelerName": "DIRECT RX",
"SubstanceName": "ATORVASTATIN CALCIUM",
"StrengthNumber": "40",
"StrengthUnit": "mg/1",
"Pharm_Classes": "HMG-CoA Reductase Inhibitor [EPC],Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]",
"DEASchedule": null,
"Status": "Deprecated",
"LastUpdate": "2020-01-01",
"PackageNdcExcludeFlag": "N",
"ProductNdcExcludeFlag": "N",
"ListingRecordCertifiedThrough": "20191231",
"StartMarketingDatePackage": "20180314",
"EndMarketingDatePackage": null,
"SamplePackage": "N"
}
}