{
"NDC": {
"NDCCode": "70882-111-20",
"PackageDescription": "20 TABLET, FILM COATED in 1 BLISTER PACK (70882-111-20)",
"NDC11Code": "70882-0111-20",
"ProductNDC": "70882-111",
"ProductTypeName": "HUMAN PRESCRIPTION DRUG",
"ProprietaryName": "Amoxicillin And Clavulanate Potassium",
"ProprietaryNameSuffix": null,
"NonProprietaryName": "Amoxicillin And Clavulanate Potassium",
"DosageFormName": "TABLET, FILM COATED",
"RouteName": "ORAL",
"StartMarketingDate": "20050823",
"EndMarketingDate": null,
"MarketingCategoryName": "ANDA",
"ApplicationNumber": "ANDA065189",
"LabelerName": "Cambridge Therapeutics Technologies, LLC",
"SubstanceName": "AMOXICILLIN; CLAVULANATE POTASSIUM",
"StrengthNumber": "250; 125",
"StrengthUnit": "mg/1; mg/1",
"Pharm_Classes": "Penicillin-class Antibacterial [EPC], Penicillins [CS], beta Lactamase Inhibitor [EPC], beta Lactamase Inhibitors [MoA]",
"DEASchedule": null,
"Status": "Active",
"LastUpdate": "2016-12-22",
"PackageNdcExcludeFlag": "N",
"ProductNdcExcludeFlag": "N",
"ListingRecordCertifiedThrough": "20261231",
"StartMarketingDatePackage": "20050823",
"EndMarketingDatePackage": null,
"SamplePackage": "N"
}
}