{
"NDC": {
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"PackageDescription": "50 BLISTER PACK in 1 BOX, UNIT-DOSE (62584-163-65) / 1 TABLET in 1 BLISTER PACK (62584-163-11) ",
"NDC11Code": "62584-0163-65",
"ProductNDC": "62584-163",
"ProductTypeName": "HUMAN PRESCRIPTION DRUG",
"ProprietaryName": "Demeclocycline Hydrochloride",
"ProprietaryNameSuffix": null,
"NonProprietaryName": "Demeclocycline Hydrochloride",
"DosageFormName": "TABLET",
"RouteName": "ORAL",
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"EndMarketingDate": "20231031",
"MarketingCategoryName": "ANDA",
"ApplicationNumber": "ANDA065425",
"LabelerName": "American Health Packaging",
"SubstanceName": "DEMECLOCYCLINE HYDROCHLORIDE",
"StrengthNumber": "300",
"StrengthUnit": "mg/1",
"Pharm_Classes": "Tetracycline-class Antimicrobial [EPC], Tetracyclines [CS]",
"DEASchedule": null,
"Status": "Deprecated",
"LastUpdate": "2023-11-01",
"PackageNdcExcludeFlag": "N",
"ProductNdcExcludeFlag": "N",
"ListingRecordCertifiedThrough": null,
"StartMarketingDatePackage": "20101209",
"EndMarketingDatePackage": "20231031",
"SamplePackage": "N"
}
}