79903-005-27 : NDC 2026 Code

79903-005-27 : Naproxen Sodium ( All Day Pain Relief )

Additionally :

You can get information about “79903-005-27” NDC code in 79903-005-27 in HTML format

HTML | 79903-005-27 in TXT (Plain Text) format

TXT | 79903-005-27 in PDF (Portable Document Format)

PDF | 79903-005-27 in XML format

XML formats.

NDC Code : 79903-005-27 – JSON Data Format

                
{
  "NDC": {
    "NDCCode": "79903-005-27",
    "PackageDescription": "270 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (79903-005-27) ",
    "NDC11Code": "79903-0005-27",
    "ProductNDC": "79903-005",
    "ProductTypeName": "HUMAN OTC DRUG",
    "ProprietaryName": "All Day Pain Relief",
    "ProprietaryNameSuffix": null,
    "NonProprietaryName": "Naproxen Sodium",
    "DosageFormName": "TABLET, FILM COATED",
    "RouteName": "ORAL",
    "StartMarketingDate": "20201022",
    "EndMarketingDate": null,
    "MarketingCategoryName": "ANDA",
    "ApplicationNumber": "ANDA204872",
    "LabelerName": "WALMART INC.",
    "SubstanceName": "NAPROXEN SODIUM",
    "StrengthNumber": "220",
    "StrengthUnit": "mg/1",
    "Pharm_Classes": "Anti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Nonsteroidal Anti-inflammatory Drug [EPC]",
    "DEASchedule": null,
    "Status": "Active",
    "LastUpdate": "2025-12-16",
    "PackageNdcExcludeFlag": "N",
    "ProductNdcExcludeFlag": "N",
    "ListingRecordCertifiedThrough": "20261231",
    "StartMarketingDatePackage": "20201022",
    "EndMarketingDatePackage": null,
    "SamplePackage": "N"
  }
}