60687-569-01 : NDC 2026 Code

60687-569-01 : Diphenoxylate Hydrochloride And Atropine Sulfate ( Diphenoxylate Hydrochloride And Atropine Sulfate )

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NDC Code : 60687-569-01 – JSON Data Format

                
{
  "NDC": {
    "NDCCode": "60687-569-01",
    "PackageDescription": "100 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-569-01)  &gt; 1 TABLET in 1 BLISTER PACK (60687-569-11) ",
    "NDC11Code": "60687-0569-01",
    "ProductNDC": "60687-569",
    "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
    "ProprietaryName": "Diphenoxylate Hydrochloride And Atropine Sulfate",
    "ProprietaryNameSuffix": null,
    "NonProprietaryName": "Diphenoxylate Hydrochloride And Atropine Sulfate",
    "DosageFormName": "TABLET",
    "RouteName": "ORAL",
    "StartMarketingDate": "20201001",
    "EndMarketingDate": "20220831",
    "MarketingCategoryName": "ANDA",
    "ApplicationNumber": "ANDA085372",
    "LabelerName": "American Health Packaging",
    "SubstanceName": "ATROPINE SULFATE; DIPHENOXYLATE HYDROCHLORIDE",
    "StrengthNumber": ".025; 2.5",
    "StrengthUnit": "mg/1; mg/1",
    "Pharm_Classes": "Anticholinergic [EPC], Antidiarrheal [EPC], Cholinergic Antagonists [MoA], Cholinergic Muscarinic Antagonist [EPC], Cholinergic Muscarinic Antagonists [MoA]",
    "DEASchedule": "CV",
    "Status": "Deprecated",
    "LastUpdate": "2022-09-01",
    "PackageNdcExcludeFlag": "N",
    "ProductNdcExcludeFlag": "N",
    "ListingRecordCertifiedThrough": null,
    "StartMarketingDatePackage": "20201001",
    "EndMarketingDatePackage": "20220831",
    "SamplePackage": "N"
  }
}