{
"NDC": {
"NDCCode": "76333-159-12",
"PackageDescription": "1000 TABLET, FILM COATED in 1 BOTTLE (76333-159-12) ",
"NDC11Code": "76333-0159-12",
"ProductNDC": "76333-159",
"ProductTypeName": "HUMAN PRESCRIPTION DRUG",
"ProprietaryName": "Pitavastatin",
"ProprietaryNameSuffix": null,
"NonProprietaryName": "Pitavastatin Calcium",
"DosageFormName": "TABLET, FILM COATED",
"RouteName": "ORAL",
"StartMarketingDate": "20160129",
"EndMarketingDate": null,
"MarketingCategoryName": "ANDA",
"ApplicationNumber": "ANDA205932",
"LabelerName": "Orient Pharma Co., Ltd.",
"SubstanceName": "PITAVASTATIN CALCIUM",
"StrengthNumber": "4.18",
"StrengthUnit": "mg/1",
"Pharm_Classes": "HMG-CoA Reductase Inhibitor [EPC],Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]",
"DEASchedule": null,
"Status": "Deprecated",
"LastUpdate": "2018-06-29",
"PackageNdcExcludeFlag": "N",
"ProductNdcExcludeFlag": "N",
"ListingRecordCertifiedThrough": "20191231",
"StartMarketingDatePackage": "20160129",
"EndMarketingDatePackage": null,
"SamplePackage": "N"
}
}