51754-1000-4 : NDC 2026 Code

51754-1000-4 : Magnesium Sulfate Heptahydrate ( Magnesium Sulfate )

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NDC Code : 51754-1000-4 – JSON Data Format

                
{
  "NDC": {
    "NDCCode": "51754-1000-4",
    "PackageDescription": "25 VIAL, SINGLE-DOSE in 1 TRAY (51754-1000-4)  &gt; 10 mL in 1 VIAL, SINGLE-DOSE",
    "NDC11Code": "51754-1000-04",
    "ProductNDC": "51754-1000",
    "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
    "ProprietaryName": "Magnesium Sulfate",
    "ProprietaryNameSuffix": null,
    "NonProprietaryName": "Magnesium Sulfate Heptahydrate",
    "DosageFormName": "INJECTION, SOLUTION",
    "RouteName": "INTRAMUSCULAR; INTRAVENOUS",
    "StartMarketingDate": "20140223",
    "EndMarketingDate": null,
    "MarketingCategoryName": "ANDA",
    "ApplicationNumber": "ANDA206039",
    "LabelerName": "Exela Pharma Sciences, LLC",
    "SubstanceName": "MAGNESIUM SULFATE HEPTAHYDRATE",
    "StrengthNumber": "500",
    "StrengthUnit": "mg/mL",
    "Pharm_Classes": "Calculi Dissolution Agent [EPC], Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Inhibition Small Intestine Fluid/Electrolyte Absorption [PE], Magnesium Ion Exchange Activity [MoA], Osmotic Activity [MoA], Osmotic Laxative [EPC], Stimulation Large Intestine Fluid/Electrolyte Secretion [PE]",
    "DEASchedule": null,
    "Status": "Deprecated",
    "LastUpdate": "2025-01-01",
    "PackageNdcExcludeFlag": "N",
    "ProductNdcExcludeFlag": "N",
    "ListingRecordCertifiedThrough": "20241231",
    "StartMarketingDatePackage": "20140223",
    "EndMarketingDatePackage": null,
    "SamplePackage": "N"
  }
}