51662-1342-1 : NDC 2025 Code

51662-1342-1 : Sodium Chloride ( Sodium Chloride )

Additionally :

You can get information about “51662-1342-1” NDC code in 51662-1342-1 in HTML format

HTML | 51662-1342-1 in TXT (Plain Text) format

TXT | 51662-1342-1 in PDF (Portable Document Format)

PDF | 51662-1342-1 in XML format

XML formats.

NDC Code : 51662-1342-1 – JSON Data Format

                
{
  "NDC": {
    "NDCCode": "51662-1342-1",
    "PackageDescription": "10 mL in 1 VIAL, SINGLE-DOSE (51662-1342-1) ",
    "NDC11Code": "51662-1342-01",
    "ProductNDC": "51662-1342",
    "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
    "ProprietaryName": "Sodium Chloride",
    "ProprietaryNameSuffix": null,
    "NonProprietaryName": "Sodium Chloride",
    "DosageFormName": "INJECTION, SOLUTION",
    "RouteName": "INTRAMUSCULAR; INTRAVENOUS; SUBCUTANEOUS",
    "StartMarketingDate": "20181222",
    "EndMarketingDate": null,
    "MarketingCategoryName": "NDA",
    "ApplicationNumber": "NDA018803",
    "LabelerName": "HF Acquisition Co LLC, DBA HealthFirst",
    "SubstanceName": "SODIUM CHLORIDE",
    "StrengthNumber": "9",
    "StrengthUnit": "mg/mL",
    "Pharm_Classes": "Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Osmotic Activity [MoA], Osmotic Laxative [EPC]",
    "DEASchedule": null,
    "Status": "Active",
    "LastUpdate": "2025-01-10",
    "PackageNdcExcludeFlag": "N",
    "ProductNdcExcludeFlag": "N",
    "ListingRecordCertifiedThrough": "20261231",
    "StartMarketingDatePackage": "20181222",
    "EndMarketingDatePackage": null,
    "SamplePackage": "N"
  }
}