{
"NDC": {
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"PackageDescription": "14 TABLET, FILM COATED in 1 BLISTER PACK (54458-849-14)",
"NDC11Code": "54458-0849-14",
"ProductNDC": "54458-849",
"ProductTypeName": "HUMAN OTC DRUG",
"ProprietaryName": "Loperamide Hydrochloride",
"ProprietaryNameSuffix": null,
"NonProprietaryName": "Loperamide Hcl",
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"RouteName": "ORAL",
"StartMarketingDate": "20160601",
"EndMarketingDate": null,
"MarketingCategoryName": "ANDA",
"ApplicationNumber": "ANDA075232",
"LabelerName": "International Laboratories, LLC",
"SubstanceName": "LOPERAMIDE HYDROCHLORIDE",
"StrengthNumber": "2",
"StrengthUnit": "mg/1",
"Pharm_Classes": null,
"DEASchedule": null,
"Status": "Deprecated",
"LastUpdate": "2018-11-09",
"PackageNdcExcludeFlag": null,
"ProductNdcExcludeFlag": "N",
"ListingRecordCertifiedThrough": "20181231",
"StartMarketingDatePackage": null,
"EndMarketingDatePackage": null,
"SamplePackage": null
}
}