{
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"PackageDescription": "20 TABLET, FILM COATED in 1 BOTTLE (68047-713-20) ",
"NDC11Code": "68047-0713-20",
"ProductNDC": "68047-713",
"ProductTypeName": "HUMAN PRESCRIPTION DRUG",
"ProprietaryName": "Ofloxacin",
"ProprietaryNameSuffix": null,
"NonProprietaryName": "Ofloxacin",
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"StartMarketingDate": "20140520",
"EndMarketingDate": "20230531",
"MarketingCategoryName": "ANDA",
"ApplicationNumber": "ANDA076093",
"LabelerName": "Larken Laboratories, Inc.",
"SubstanceName": "OFLOXACIN",
"StrengthNumber": "400",
"StrengthUnit": "mg/1",
"Pharm_Classes": "Quinolone Antimicrobial [EPC], Quinolones [CS]",
"DEASchedule": null,
"Status": "Deprecated",
"LastUpdate": "2023-06-01",
"PackageNdcExcludeFlag": "N",
"ProductNdcExcludeFlag": "N",
"ListingRecordCertifiedThrough": null,
"StartMarketingDatePackage": "20200819",
"EndMarketingDatePackage": "20230531",
"SamplePackage": "N"
}
}