68788-7021-2 : NDC 2026 Code

68788-7021-2 : Diphenoxylate Hydrochloride And Atropine Sulfate ( Diphenoxylate Hydrochloride And Atropine Sulfate )

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NDC Code : 68788-7021-2 – JSON Data Format

                
{
  "NDC": {
    "NDCCode": "68788-7021-2",
    "PackageDescription": "20 TABLET in 1 BOTTLE (68788-7021-2) ",
    "NDC11Code": "68788-7021-02",
    "ProductNDC": "68788-7021",
    "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
    "ProprietaryName": "Diphenoxylate Hydrochloride And Atropine Sulfate",
    "ProprietaryNameSuffix": null,
    "NonProprietaryName": "Diphenoxylate Hydrochloride And Atropine Sulfate",
    "DosageFormName": "TABLET",
    "RouteName": "ORAL",
    "StartMarketingDate": "20171011",
    "EndMarketingDate": null,
    "MarketingCategoryName": "ANDA",
    "ApplicationNumber": "ANDA086727",
    "LabelerName": "Preferred Pharmaceuticals Inc.",
    "SubstanceName": "DIPHENOXYLATE HYDROCHLORIDE; ATROPINE SULFATE",
    "StrengthNumber": "2.5; .025",
    "StrengthUnit": "mg/1; mg/1",
    "Pharm_Classes": "Antidiarrheal [EPC],Anticholinergic [EPC],Cholinergic Antagonists [MoA],Cholinergic Muscarinic Antagonist [EPC],Cholinergic Muscarinic Antagonists [MoA]",
    "DEASchedule": "CV",
    "Status": "Deprecated",
    "LastUpdate": "2021-04-29",
    "PackageNdcExcludeFlag": "N",
    "ProductNdcExcludeFlag": "N",
    "ListingRecordCertifiedThrough": "20211231",
    "StartMarketingDatePackage": "20171011",
    "EndMarketingDatePackage": null,
    "SamplePackage": "N"
  }
}