{
"NDC": {
"NDCCode": "70518-1656-0",
"PackageDescription": "30 TABLET in 1 BLISTER PACK (70518-1656-0) ",
"NDC11Code": "70518-1656-00",
"ProductNDC": "70518-1656",
"ProductTypeName": "HUMAN PRESCRIPTION DRUG",
"ProprietaryName": "Zidovudine",
"ProprietaryNameSuffix": null,
"NonProprietaryName": "Zidovudine",
"DosageFormName": "TABLET",
"RouteName": "ORAL",
"StartMarketingDate": "20181108",
"EndMarketingDate": null,
"MarketingCategoryName": "ANDA",
"ApplicationNumber": "ANDA090092",
"LabelerName": "REMEDYREPACK INC.",
"SubstanceName": "ZIDOVUDINE",
"StrengthNumber": "300",
"StrengthUnit": "mg/1",
"Pharm_Classes": "Human Immunodeficiency Virus Nucleoside Analog Reverse Transcriptase Inhibitor [EPC], Nucleoside Reverse Transcriptase Inhibitors [MoA]",
"DEASchedule": null,
"Status": "Deprecated",
"LastUpdate": "2024-06-13",
"PackageNdcExcludeFlag": "N",
"ProductNdcExcludeFlag": "N",
"ListingRecordCertifiedThrough": "20251231",
"StartMarketingDatePackage": "20181108",
"EndMarketingDatePackage": null,
"SamplePackage": "N"
}
}