63739-325-10 : NDC 2026 Code

63739-325-10 : Famotidine ( Famotidine )

Additionally :

You can get information about “63739-325-10” NDC code in 63739-325-10 in HTML format

HTML | 63739-325-10 in TXT (Plain Text) format

TXT | 63739-325-10 in PDF (Portable Document Format)

PDF | 63739-325-10 in XML format

XML formats.

NDC Code : 63739-325-10 – JSON Data Format

                
{
  "NDC": {
    "NDCCode": "63739-325-10",
    "PackageDescription": "10 BLISTER PACK in 1 BOX, UNIT-DOSE (63739-325-10)  &gt; 10 TABLET, FILM COATED in 1 BLISTER PACK",
    "NDC11Code": "63739-0325-10",
    "ProductNDC": "63739-325",
    "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
    "ProprietaryName": "Famotidine",
    "ProprietaryNameSuffix": null,
    "NonProprietaryName": "Famotidine",
    "DosageFormName": "TABLET, FILM COATED",
    "RouteName": "ORAL",
    "StartMarketingDate": "20010416",
    "EndMarketingDate": null,
    "MarketingCategoryName": "ANDA",
    "ApplicationNumber": "ANDA075718",
    "LabelerName": "McKesson Corporation",
    "SubstanceName": "FAMOTIDINE",
    "StrengthNumber": "20",
    "StrengthUnit": "mg/1",
    "Pharm_Classes": "Histamine H2 Receptor Antagonists [MoA],Histamine-2 Receptor Antagonist [EPC]",
    "DEASchedule": null,
    "Status": "Deprecated",
    "LastUpdate": "2020-01-01",
    "PackageNdcExcludeFlag": "N",
    "ProductNdcExcludeFlag": "N",
    "ListingRecordCertifiedThrough": "20191231",
    "StartMarketingDatePackage": "20010416",
    "EndMarketingDatePackage": null,
    "SamplePackage": "N"
  }
}