60687-672-65 : NDC 2026 Code

60687-672-65 : Butalbital, Acetaminophen, And Caffeine ( Butalbital, Acetaminophen And Caffeine )

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NDC Code : 60687-672-65 – JSON Data Format

                
{
  "NDC": {
    "NDCCode": "60687-672-65",
    "PackageDescription": "50 BLISTER PACK in 1 CARTON (60687-672-65)  / 1 TABLET in 1 BLISTER PACK (60687-672-11) ",
    "NDC11Code": "60687-0672-65",
    "ProductNDC": "60687-672",
    "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
    "ProprietaryName": "Butalbital, Acetaminophen And Caffeine",
    "ProprietaryNameSuffix": null,
    "NonProprietaryName": "Butalbital, Acetaminophen, And Caffeine",
    "DosageFormName": "TABLET",
    "RouteName": "ORAL",
    "StartMarketingDate": "20221017",
    "EndMarketingDate": "20260731",
    "MarketingCategoryName": "ANDA",
    "ApplicationNumber": "ANDA040511",
    "LabelerName": "American Health Packaging",
    "SubstanceName": "ACETAMINOPHEN; BUTALBITAL; CAFFEINE",
    "StrengthNumber": "325; 50; 40",
    "StrengthUnit": "mg/1; mg/1; mg/1",
    "Pharm_Classes": "Barbiturate [EPC], Barbiturates [CS], Central Nervous System Stimulant [EPC], Central Nervous System Stimulation [PE], Methylxanthine [EPC], Xanthines [CS]",
    "DEASchedule": "CIII",
    "Status": "Active",
    "LastUpdate": "2025-09-17",
    "PackageNdcExcludeFlag": "N",
    "ProductNdcExcludeFlag": "N",
    "ListingRecordCertifiedThrough": null,
    "StartMarketingDatePackage": "20221017",
    "EndMarketingDatePackage": "20260731",
    "SamplePackage": "N"
  }
}