63739-072-33 : NDC 2026 Code

63739-072-33 : Sildenafil ( Sildenafil )

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NDC Code : 63739-072-33 – JSON Data Format

                
{
  "NDC": {
    "NDCCode": "63739-072-33",
    "PackageDescription": "3 BLISTER PACK in 1 BOX, UNIT-DOSE (63739-072-33)  / 10 TABLET, FILM COATED in 1 BLISTER PACK",
    "NDC11Code": "63739-0072-33",
    "ProductNDC": "63739-072",
    "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
    "ProprietaryName": "Sildenafil",
    "ProprietaryNameSuffix": null,
    "NonProprietaryName": "Sildenafil",
    "DosageFormName": "TABLET, FILM COATED",
    "RouteName": "ORAL",
    "StartMarketingDate": "20220329",
    "EndMarketingDate": "20250930",
    "MarketingCategoryName": "ANDA",
    "ApplicationNumber": "ANDA203623",
    "LabelerName": "McKesson Corporation dba SKY Packaging",
    "SubstanceName": "SILDENAFIL CITRATE",
    "StrengthNumber": "20",
    "StrengthUnit": "mg/1",
    "Pharm_Classes": "Phosphodiesterase 5 Inhibitor [EPC], Phosphodiesterase 5 Inhibitors [MoA]",
    "DEASchedule": null,
    "Status": "Deprecated",
    "LastUpdate": "2025-10-01",
    "PackageNdcExcludeFlag": "N",
    "ProductNdcExcludeFlag": "N",
    "ListingRecordCertifiedThrough": null,
    "StartMarketingDatePackage": "20220329",
    "EndMarketingDatePackage": "20250930",
    "SamplePackage": "N"
  }
}