42708-081-20 : NDC 2026 Code

42708-081-20 : Cyclobenzaprine Hydrochloride ( Cyclobenzaprine Hydrochloride )

Additionally :

You can get information about “42708-081-20” NDC code in 42708-081-20 in HTML format

HTML | 42708-081-20 in TXT (Plain Text) format

TXT | 42708-081-20 in PDF (Portable Document Format)

PDF | 42708-081-20 in XML format

XML formats.

NDC Code : 42708-081-20 – JSON Data Format

                
{
  "NDC": {
    "NDCCode": "42708-081-20",
    "PackageDescription": "20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (42708-081-20) ",
    "NDC11Code": "42708-0081-20",
    "ProductNDC": "42708-081",
    "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
    "ProprietaryName": "Cyclobenzaprine Hydrochloride",
    "ProprietaryNameSuffix": null,
    "NonProprietaryName": "Cyclobenzaprine Hydrochloride",
    "DosageFormName": "TABLET, FILM COATED",
    "RouteName": "ORAL",
    "StartMarketingDate": "20060203",
    "EndMarketingDate": null,
    "MarketingCategoryName": "ANDA",
    "ApplicationNumber": "ANDA071611",
    "LabelerName": "QPharma Inc",
    "SubstanceName": "CYCLOBENZAPRINE HYDROCHLORIDE",
    "StrengthNumber": "5",
    "StrengthUnit": "mg/1",
    "Pharm_Classes": "Centrally-mediated Muscle Relaxation [PE], Muscle Relaxant [EPC]",
    "DEASchedule": null,
    "Status": "Deprecated",
    "LastUpdate": "2023-12-16",
    "PackageNdcExcludeFlag": "N",
    "ProductNdcExcludeFlag": "N",
    "ListingRecordCertifiedThrough": "20231231",
    "StartMarketingDatePackage": "20190305",
    "EndMarketingDatePackage": null,
    "SamplePackage": "Y"
  }
}