60687-280-32 : NDC 2026 Code

60687-280-32 : Nifedipine ( Nifedipine )

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NDC Code : 60687-280-32 – JSON Data Format

                
{
  "NDC": {
    "NDCCode": "60687-280-32",
    "PackageDescription": "20 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-280-32)  &gt; 1 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (60687-280-33) ",
    "NDC11Code": "60687-0280-32",
    "ProductNDC": "60687-280",
    "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
    "ProprietaryName": "Nifedipine",
    "ProprietaryNameSuffix": null,
    "NonProprietaryName": "Nifedipine",
    "DosageFormName": "TABLET, FILM COATED, EXTENDED RELEASE",
    "RouteName": "ORAL",
    "StartMarketingDate": "20170223",
    "EndMarketingDate": "20190131",
    "MarketingCategoryName": "ANDA",
    "ApplicationNumber": "ANDA077899",
    "LabelerName": "American Health Packaging",
    "SubstanceName": "NIFEDIPINE",
    "StrengthNumber": "60",
    "StrengthUnit": "mg/1",
    "Pharm_Classes": "Calcium Channel Antagonists [MoA],Dihydropyridine Calcium Channel Blocker [EPC],Dihydropyridines [CS]",
    "DEASchedule": null,
    "Status": "Deprecated",
    "LastUpdate": "2019-02-01",
    "PackageNdcExcludeFlag": "N",
    "ProductNdcExcludeFlag": "N",
    "ListingRecordCertifiedThrough": null,
    "StartMarketingDatePackage": "20170223",
    "EndMarketingDatePackage": "20190131",
    "SamplePackage": "N"
  }
}