{
"NDC": {
"NDCCode": "43063-442-09",
"PackageDescription": "9 TABLET in 1 BOTTLE, PLASTIC (43063-442-09) ",
"NDC11Code": "43063-0442-09",
"ProductNDC": "43063-442",
"ProductTypeName": "HUMAN PRESCRIPTION DRUG",
"ProprietaryName": "Triamterene Hydrochlorothiazide",
"ProprietaryNameSuffix": null,
"NonProprietaryName": "Triamterene And Hydrochlorothiazide",
"DosageFormName": "TABLET",
"RouteName": "ORAL",
"StartMarketingDate": "19880617",
"EndMarketingDate": "20201130",
"MarketingCategoryName": "ANDA",
"ApplicationNumber": "ANDA072011",
"LabelerName": "PD-Rx Pharmaceuticals, Inc.",
"SubstanceName": "TRIAMTERENE; HYDROCHLOROTHIAZIDE",
"StrengthNumber": "75; 50",
"StrengthUnit": "mg/1; mg/1",
"Pharm_Classes": "Decreased Renal K+ Excretion [PE],Increased Diuresis [PE],Potassium-sparing Diuretic [EPC],Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [CS]",
"DEASchedule": null,
"Status": "Deprecated",
"LastUpdate": "2020-12-01",
"PackageNdcExcludeFlag": "N",
"ProductNdcExcludeFlag": "N",
"ListingRecordCertifiedThrough": null,
"StartMarketingDatePackage": "20120423",
"EndMarketingDatePackage": "20201130",
"SamplePackage": "N"
}
}