68071-3859-3 : NDC 2026 Code

68071-3859-3 : Methocarbamol ( Methocarbamol )

Additionally :

You can get information about “68071-3859-3” NDC code in 68071-3859-3 in HTML format

HTML | 68071-3859-3 in TXT (Plain Text) format

TXT | 68071-3859-3 in PDF (Portable Document Format)

PDF | 68071-3859-3 in XML format

XML formats.

NDC Code : 68071-3859-3 – JSON Data Format

                
{
  "NDC": {
    "NDCCode": "68071-3859-3",
    "PackageDescription": "30 TABLET, FILM COATED in 1 BOTTLE (68071-3859-3) ",
    "NDC11Code": "68071-3859-03",
    "ProductNDC": "68071-3859",
    "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
    "ProprietaryName": "Methocarbamol",
    "ProprietaryNameSuffix": null,
    "NonProprietaryName": "Methocarbamol",
    "DosageFormName": "TABLET, FILM COATED",
    "RouteName": "ORAL",
    "StartMarketingDate": "20200812",
    "EndMarketingDate": null,
    "MarketingCategoryName": "ANDA",
    "ApplicationNumber": "ANDA213967",
    "LabelerName": "NuCare Pharmaceuticals,Inc.",
    "SubstanceName": "METHOCARBAMOL",
    "StrengthNumber": "750",
    "StrengthUnit": "mg/1",
    "Pharm_Classes": "Centrally-mediated Muscle Relaxation [PE], Muscle Relaxant [EPC]",
    "DEASchedule": null,
    "Status": "Active",
    "LastUpdate": "2025-12-25",
    "PackageNdcExcludeFlag": "N",
    "ProductNdcExcludeFlag": "N",
    "ListingRecordCertifiedThrough": "20261231",
    "StartMarketingDatePackage": "20251224",
    "EndMarketingDatePackage": null,
    "SamplePackage": "N"
  }
}