{
"NDC": {
"NDCCode": "0409-9257-39",
"PackageDescription": "12 POUCH in 1 CASE (0409-9257-39) > 1 BAG in 1 POUCH > 1000 mL in 1 BAG",
"NDC11Code": "00409-9257-39",
"ProductNDC": "0409-9257",
"ProductTypeName": "HUMAN PRESCRIPTION DRUG",
"ProprietaryName": "Potassium Chloride In Sodium Chloride",
"ProprietaryNameSuffix": null,
"NonProprietaryName": "Sodium Chloride And Potassium Chloride",
"DosageFormName": "INJECTION, SOLUTION",
"RouteName": "INTRAVENOUS",
"StartMarketingDate": "20081205",
"EndMarketingDate": "20200901",
"MarketingCategoryName": "ANDA",
"ApplicationNumber": "ANDA078446",
"LabelerName": "Hospira, Inc.",
"SubstanceName": "SODIUM CHLORIDE; POTASSIUM CHLORIDE",
"StrengthNumber": "4.5; 1.49",
"StrengthUnit": "g/1000mL; g/1000mL",
"Pharm_Classes": "Osmotic Laxative [EPC],Increased Large Intestinal Motility [PE],Inhibition Large Intestine Fluid/Electrolyte Absorption [PE],Osmotic Activity [MoA],Potassium Compounds [CS],Potassium Salt [EPC],Osmotic Laxative [EPC],Increased Large Intestinal Motility [PE],Inhibition Large Intestine Fluid/Electrolyte Absorption [PE],Osmotic Activity [MoA]",
"DEASchedule": null,
"Status": "Deprecated",
"LastUpdate": "2020-09-02",
"PackageNdcExcludeFlag": "N",
"ProductNdcExcludeFlag": "N",
"ListingRecordCertifiedThrough": null,
"StartMarketingDatePackage": "20081205",
"EndMarketingDatePackage": "20200901",
"SamplePackage": "N"
}
}