{
"NDC": {
"NDCCode": "51754-2004-4",
"PackageDescription": "25 VIAL, GLASS in 1 CARTON (51754-2004-4) / 100 mL in 1 VIAL, GLASS",
"NDC11Code": "51754-2004-04",
"ProductNDC": "51754-2004",
"ProductTypeName": "HUMAN PRESCRIPTION DRUG",
"ProprietaryName": "Potassium Acetate",
"ProprietaryNameSuffix": null,
"NonProprietaryName": "Potassium Acetate",
"DosageFormName": "INJECTION",
"RouteName": "INTRAVENOUS",
"StartMarketingDate": "20230801",
"EndMarketingDate": null,
"MarketingCategoryName": "ANDA",
"ApplicationNumber": "ANDA206203",
"LabelerName": "Exela Pharma Sciences, LLC",
"SubstanceName": "POTASSIUM ACETATE",
"StrengthNumber": "200",
"StrengthUnit": "meq/100mL",
"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": "2023-08-12",
"PackageNdcExcludeFlag": "N",
"ProductNdcExcludeFlag": "N",
"ListingRecordCertifiedThrough": "20251231",
"StartMarketingDatePackage": "20230801",
"EndMarketingDatePackage": null,
"SamplePackage": "N"
}
}