53209-1004-2 : NDC 2026 Code

53209-1004-2 : Acetaminophen, Guaifenesin, And Phenylephrine Hydrochloride ( Tylenol Sinus Severe )

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NDC Code : 53209-1004-2 – JSON Data Format

                
{
  "NDC": {
    "NDCCode": "53209-1004-2",
    "PackageDescription": "25 BLISTER PACK in 1 POUCH (53209-1004-2)  / 2 TABLET, COATED in 1 BLISTER PACK (53209-1004-1) ",
    "NDC11Code": "53209-1004-02",
    "ProductNDC": "53209-1004",
    "ProductTypeName": "HUMAN OTC DRUG",
    "ProprietaryName": "Tylenol Sinus Severe",
    "ProprietaryNameSuffix": null,
    "NonProprietaryName": "Acetaminophen, Guaifenesin, And Phenylephrine Hydrochloride",
    "DosageFormName": "TABLET, COATED",
    "RouteName": "ORAL",
    "StartMarketingDate": "20250619",
    "EndMarketingDate": null,
    "MarketingCategoryName": "OTC MONOGRAPH DRUG",
    "ApplicationNumber": "M012",
    "LabelerName": "Morning Star OTC",
    "SubstanceName": "ACETAMINOPHEN; GUAIFENESIN; PHENYLEPHRINE HYDROCHLORIDE",
    "StrengthNumber": "325; 200; 5",
    "StrengthUnit": "mg/1; mg/1; mg/1",
    "Pharm_Classes": "Adrenergic alpha1-Agonists [MoA], Decreased Respiratory Secretion Viscosity [PE], Expectorant [EPC], Increased Respiratory Secretions [PE], alpha-1 Adrenergic Agonist [EPC]",
    "DEASchedule": null,
    "Status": "Active",
    "LastUpdate": "2025-06-21",
    "PackageNdcExcludeFlag": "N",
    "ProductNdcExcludeFlag": "N",
    "ListingRecordCertifiedThrough": "20261231",
    "StartMarketingDatePackage": "20250619",
    "EndMarketingDatePackage": null,
    "SamplePackage": "N"
  }
}