83324-149-36 : NDC 2026 Code

83324-149-36 : Acetaminophen And Ibuprofen ( Dual Action Pain Reliever )

Additionally :

You can get information about “83324-149-36” NDC code in 83324-149-36 in HTML format

HTML | 83324-149-36 in TXT (Plain Text) format

TXT | 83324-149-36 in PDF (Portable Document Format)

PDF | 83324-149-36 in XML format

XML formats.

NDC Code : 83324-149-36 – JSON Data Format

                
{
  "NDC": {
    "NDCCode": "83324-149-36",
    "PackageDescription": "1 BOTTLE in 1 CARTON (83324-149-36)  / 36 TABLET, FILM COATED in 1 BOTTLE",
    "NDC11Code": "83324-0149-36",
    "ProductNDC": "83324-149",
    "ProductTypeName": "HUMAN OTC DRUG",
    "ProprietaryName": "Dual Action Pain Reliever",
    "ProprietaryNameSuffix": null,
    "NonProprietaryName": "Acetaminophen And Ibuprofen",
    "DosageFormName": "TABLET, FILM COATED",
    "RouteName": "ORAL",
    "StartMarketingDate": "20241003",
    "EndMarketingDate": null,
    "MarketingCategoryName": "ANDA",
    "ApplicationNumber": "ANDA216999",
    "LabelerName": "CHAIN DRUG MARKETING ASSOCIATION INC.",
    "SubstanceName": "ACETAMINOPHEN; IBUPROFEN",
    "StrengthNumber": "250; 125",
    "StrengthUnit": "mg/1; mg/1",
    "Pharm_Classes": "Anti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Nonsteroidal Anti-inflammatory Drug [EPC]",
    "DEASchedule": null,
    "Status": "Active",
    "LastUpdate": "2024-10-05",
    "PackageNdcExcludeFlag": "N",
    "ProductNdcExcludeFlag": "N",
    "ListingRecordCertifiedThrough": "20261231",
    "StartMarketingDatePackage": "20241003",
    "EndMarketingDatePackage": null,
    "SamplePackage": "N"
  }
}