{
"NDC": {
"NDCCode": "51754-9995-5",
"PackageDescription": "20 VIAL in 1 CARTON (51754-9995-5) > 100 mL in 1 VIAL (51754-9995-1) ",
"NDC11Code": "51754-9995-05",
"ProductNDC": "51754-9995",
"ProductTypeName": "HUMAN PRESCRIPTION DRUG",
"ProprietaryName": "Sodium Acetate",
"ProprietaryNameSuffix": null,
"NonProprietaryName": "Sodium Acetate",
"DosageFormName": "INJECTION, SOLUTION",
"RouteName": "INTRAVENOUS",
"StartMarketingDate": "20220701",
"EndMarketingDate": null,
"MarketingCategoryName": "UNAPPROVED DRUG OTHER",
"ApplicationNumber": null,
"LabelerName": "Exela Pharma Sciences, LLC",
"SubstanceName": "SODIUM ACETATE ANHYDROUS",
"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]",
"DEASchedule": null,
"Status": "Deprecated",
"LastUpdate": "2022-12-16",
"PackageNdcExcludeFlag": "N",
"ProductNdcExcludeFlag": "N",
"ListingRecordCertifiedThrough": "20231231",
"StartMarketingDatePackage": "20220701",
"EndMarketingDatePackage": null,
"SamplePackage": "N"
}
}