37808-614-05 : NDC 2026 Code

37808-614-05 : Calcium Carbonate, Magnesium Hydroxide ( Supreme Antacid )

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NDC Code : 37808-614-05 – JSON Data Format

                
{
  "NDC": {
    "NDCCode": "37808-614-05",
    "PackageDescription": "355 mL in 1 BOTTLE (37808-614-05) ",
    "NDC11Code": "37808-0614-05",
    "ProductNDC": "37808-614",
    "ProductTypeName": "HUMAN OTC DRUG",
    "ProprietaryName": "Supreme Antacid",
    "ProprietaryNameSuffix": null,
    "NonProprietaryName": "Calcium Carbonate, Magnesium Hydroxide",
    "DosageFormName": "LIQUID",
    "RouteName": "ORAL",
    "StartMarketingDate": "20250207",
    "EndMarketingDate": null,
    "MarketingCategoryName": "OTC MONOGRAPH DRUG",
    "ApplicationNumber": "M001",
    "LabelerName": "H E B",
    "SubstanceName": "CALCIUM CARBONATE; MAGNESIUM HYDROXIDE",
    "StrengthNumber": "800; 270",
    "StrengthUnit": "mg/10mL; mg/10mL",
    "Pharm_Classes": "Blood Coagulation Factor [EPC], Calcium [CS], Calculi Dissolution Agent [EPC], Cations, Divalent [CS], Increased Coagulation Factor Activity [PE], 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], Phosphate Binder [EPC], Phosphate Chelating Activity [MoA], Stimulation Large Intestine Fluid/Electrolyte Secretion [PE]",
    "DEASchedule": null,
    "Status": "Active",
    "LastUpdate": "2025-03-17",
    "PackageNdcExcludeFlag": "N",
    "ProductNdcExcludeFlag": "N",
    "ListingRecordCertifiedThrough": "20261231",
    "StartMarketingDatePackage": "20250207",
    "EndMarketingDatePackage": null,
    "SamplePackage": "N"
  }
}