{
"NDC": {
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"PackageDescription": "100 POUCH in 1 BOX, UNIT-DOSE (17856-1135-1) / 1 TABLET, EXTENDED RELEASE in 1 POUCH",
"NDC11Code": "17856-1135-01",
"ProductNDC": "17856-1135",
"ProductTypeName": "HUMAN PRESCRIPTION DRUG",
"ProprietaryName": "Potassium Chloride Extended-release",
"ProprietaryNameSuffix": null,
"NonProprietaryName": "Potassium Chloride Extended-release",
"DosageFormName": "TABLET, EXTENDED RELEASE",
"RouteName": "ORAL",
"StartMarketingDate": "20210130",
"EndMarketingDate": null,
"MarketingCategoryName": "ANDA",
"ApplicationNumber": "ANDA214452",
"LabelerName": "Atlantic Biologicals Corp.",
"SubstanceName": "POTASSIUM CHLORIDE",
"StrengthNumber": "1500",
"StrengthUnit": "mg/1",
"Pharm_Classes": "Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Osmotic Activity [MoA], Osmotic Laxative [EPC], Potassium Compounds [CS], Potassium Salt [EPC]",
"DEASchedule": null,
"Status": "Active",
"LastUpdate": "2026-04-01",
"PackageNdcExcludeFlag": "N",
"ProductNdcExcludeFlag": "N",
"ListingRecordCertifiedThrough": "20271231",
"StartMarketingDatePackage": "20210130",
"EndMarketingDatePackage": null,
"SamplePackage": "N"
}
}