70710-1378-1 : NDC 2026 Code

70710-1378-1 : Butalbital, Acetaminophen, And Caffeine ( Butalbital, Acetaminophen, And Caffeine )

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NDC Code : 70710-1378-1 – JSON Data Format

                
{
  "NDC": {
    "NDCCode": "70710-1378-1",
    "PackageDescription": "100 TABLET in 1 BOTTLE (70710-1378-1) ",
    "NDC11Code": "70710-1378-01",
    "ProductNDC": "70710-1378",
    "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
    "ProprietaryName": "Butalbital, Acetaminophen, And Caffeine",
    "ProprietaryNameSuffix": null,
    "NonProprietaryName": "Butalbital, Acetaminophen, And Caffeine",
    "DosageFormName": "TABLET",
    "RouteName": "ORAL",
    "StartMarketingDate": "20200721",
    "EndMarketingDate": null,
    "MarketingCategoryName": "ANDA",
    "ApplicationNumber": "ANDA211543",
    "LabelerName": "Zydus Pharmaceuticals (USA) Inc.",
    "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": "Deprecated",
    "LastUpdate": "2022-08-02",
    "PackageNdcExcludeFlag": "N",
    "ProductNdcExcludeFlag": "N",
    "ListingRecordCertifiedThrough": "20221231",
    "StartMarketingDatePackage": "20200721",
    "EndMarketingDatePackage": null,
    "SamplePackage": "N"
  }
}