70518-0191-3 : NDC 2026 Code

70518-0191-3 : Cyclobenzaprine Hydrochloride ( Cyclobenzaprine Hydrochloride )

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NDC Code : 70518-0191-3 – JSON Data Format

                
{
  "NDC": {
    "NDCCode": "70518-0191-3",
    "PackageDescription": "60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-0191-3) ",
    "NDC11Code": "70518-0191-03",
    "ProductNDC": "70518-0191",
    "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
    "ProprietaryName": "Cyclobenzaprine Hydrochloride",
    "ProprietaryNameSuffix": null,
    "NonProprietaryName": "Cyclobenzaprine Hydrochloride",
    "DosageFormName": "TABLET, FILM COATED",
    "RouteName": "ORAL",
    "StartMarketingDate": "20170202",
    "EndMarketingDate": null,
    "MarketingCategoryName": "ANDA",
    "ApplicationNumber": "ANDA078048",
    "LabelerName": "REMEDYREPACK INC.",
    "SubstanceName": "CYCLOBENZAPRINE HYDROCHLORIDE",
    "StrengthNumber": "5",
    "StrengthUnit": "mg/1",
    "Pharm_Classes": "Centrally-mediated Muscle Relaxation [PE], Muscle Relaxant [EPC]",
    "DEASchedule": null,
    "Status": "Deprecated",
    "LastUpdate": "2022-08-26",
    "PackageNdcExcludeFlag": "N",
    "ProductNdcExcludeFlag": "N",
    "ListingRecordCertifiedThrough": "20231231",
    "StartMarketingDatePackage": "20210420",
    "EndMarketingDatePackage": null,
    "SamplePackage": "N"
  }
}