50268-139-13 : NDC 2026 Code

50268-139-13 : Butalbital, Acetaminophen And Caffeine ( Butalbital, Acetaminophen And Caffeine )

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NDC Code : 50268-139-13 – JSON Data Format

                
{
  "NDC": {
    "NDCCode": "50268-139-13",
    "PackageDescription": "30 BLISTER PACK in 1 BOX, UNIT-DOSE (50268-139-13)  &gt; 1 TABLET in 1 BLISTER PACK (50268-139-11) ",
    "NDC11Code": "50268-0139-13",
    "ProductNDC": "50268-139",
    "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
    "ProprietaryName": "Butalbital, Acetaminophen And Caffeine",
    "ProprietaryNameSuffix": null,
    "NonProprietaryName": "Butalbital, Acetaminophen And Caffeine",
    "DosageFormName": "TABLET",
    "RouteName": "ORAL",
    "StartMarketingDate": "20170721",
    "EndMarketingDate": null,
    "MarketingCategoryName": "ANDA",
    "ApplicationNumber": "ANDA089718",
    "LabelerName": "AvPAK",
    "SubstanceName": "BUTALBITAL; ACETAMINOPHEN; CAFFEINE",
    "StrengthNumber": "50; 325; 40",
    "StrengthUnit": "mg/1; mg/1; mg/1",
    "Pharm_Classes": "Barbiturates [CS],Barbiturate [EPC],Central Nervous System Stimulant [EPC],Methylxanthine [EPC],Xanthines [CS],Central Nervous System Stimulation [PE]",
    "DEASchedule": null,
    "Status": "Deprecated",
    "LastUpdate": "2019-10-30",
    "PackageNdcExcludeFlag": "N",
    "ProductNdcExcludeFlag": "N",
    "ListingRecordCertifiedThrough": "20191231",
    "StartMarketingDatePackage": "20170721",
    "EndMarketingDatePackage": null,
    "SamplePackage": "N"
  }
}