63739-110-01 : NDC 2026 Code

63739-110-01 : Folic Acid ( Folic Acid )

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NDC Code : 63739-110-01 – JSON Data Format

                
{
  "NDC": {
    "NDCCode": "63739-110-01",
    "PackageDescription": "25 BLISTER PACK in 1 BOX, UNIT-DOSE (63739-110-01)  &gt; 30 TABLET in 1 BLISTER PACK",
    "NDC11Code": "63739-0110-01",
    "ProductNDC": "63739-110",
    "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
    "ProprietaryName": "Folic Acid",
    "ProprietaryNameSuffix": null,
    "NonProprietaryName": "Folic Acid",
    "DosageFormName": "TABLET",
    "RouteName": "ORAL",
    "StartMarketingDate": "20041124",
    "EndMarketingDate": null,
    "MarketingCategoryName": "ANDA",
    "ApplicationNumber": "ANDA080600",
    "LabelerName": "McKesson Packaging Services Business Unit of McKesson Corporation.",
    "SubstanceName": "FOLIC ACID",
    "StrengthNumber": "1",
    "StrengthUnit": "mg/1",
    "Pharm_Classes": null,
    "DEASchedule": null,
    "Status": "Deprecated",
    "LastUpdate": "2015-06-16",
    "PackageNdcExcludeFlag": null,
    "ProductNdcExcludeFlag": null,
    "ListingRecordCertifiedThrough": null,
    "StartMarketingDatePackage": null,
    "EndMarketingDatePackage": null,
    "SamplePackage": null
  }
}