75826-107-00 : NDC 2026 Code

75826-107-00 : Diphenoxylate Hydrochloride And Atropine Sulfate ( Diphenoxylate Hydrochloride And Atropine Sulfate )

Additionally :

You can get information about “75826-107-00” NDC code in 75826-107-00 in HTML format

HTML | 75826-107-00 in TXT (Plain Text) format

TXT | 75826-107-00 in PDF (Portable Document Format)

PDF | 75826-107-00 in XML format

XML formats.

NDC Code : 75826-107-00 – JSON Data Format

                
{
  "NDC": {
    "NDCCode": "75826-107-00",
    "PackageDescription": "1000 TABLET in 1 BOTTLE, PLASTIC (75826-107-00) ",
    "NDC11Code": "75826-0107-00",
    "ProductNDC": "75826-107",
    "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
    "ProprietaryName": "Diphenoxylate Hydrochloride And Atropine Sulfate",
    "ProprietaryNameSuffix": null,
    "NonProprietaryName": "Diphenoxylate Hydrochloride And Atropine Sulfate",
    "DosageFormName": "TABLET",
    "RouteName": "ORAL",
    "StartMarketingDate": "20220430",
    "EndMarketingDate": null,
    "MarketingCategoryName": "ANDA",
    "ApplicationNumber": "ANDA211362",
    "LabelerName": "Winder Laboratories LLC",
    "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": "Active",
    "LastUpdate": "2025-01-08",
    "PackageNdcExcludeFlag": "N",
    "ProductNdcExcludeFlag": "N",
    "ListingRecordCertifiedThrough": "20261231",
    "StartMarketingDatePackage": "20220901",
    "EndMarketingDatePackage": null,
    "SamplePackage": "N"
  }
}