63083-6021-2 : NDC 2026 Code

63083-6021-2 : Mytox ( Mytox )

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NDC Code : 63083-6021-2 – JSON Data Format

                
{
  "NDC": {
    "NDCCode": "63083-6021-2",
    "PackageDescription": "59 mL in 1 BOTTLE, DROPPER (63083-6021-2) ",
    "NDC11Code": "63083-6021-02",
    "ProductNDC": "63083-6021",
    "ProductTypeName": "HUMAN OTC DRUG",
    "ProprietaryName": "Mytox",
    "ProprietaryNameSuffix": "6021",
    "NonProprietaryName": "Mytox",
    "DosageFormName": "LIQUID",
    "RouteName": "ORAL",
    "StartMarketingDate": "19840815",
    "EndMarketingDate": null,
    "MarketingCategoryName": "UNAPPROVED HOMEOPATHIC",
    "ApplicationNumber": null,
    "LabelerName": "Professional Complementary Health Formulas",
    "SubstanceName": "AMANITA MUSCARIA FRUITING BODY; ARSENIC TRIOXIDE; BUFO BUFO CUTANEOUS GLAND; COLCHICUM AUTUMNALE BULB; DROSERA ROTUNDIFOLIA WHOLE; SODIUM BORATE; UBIDECARENONE",
    "StrengthNumber": "6; 6; 8; 4; 6; 4; 12",
    "StrengthUnit": "[hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL; [hp_X]/59mL",
    "Pharm_Classes": null,
    "DEASchedule": null,
    "Status": "Active",
    "LastUpdate": "2026-01-13",
    "PackageNdcExcludeFlag": "N",
    "ProductNdcExcludeFlag": "N",
    "ListingRecordCertifiedThrough": "20271231",
    "StartMarketingDatePackage": "19850815",
    "EndMarketingDatePackage": null,
    "SamplePackage": "N"
  }
}