76420-007-05 : NDC 2026 Code

76420-007-05 : Betamethasone Sodium Phosphate And Betamethasone Acetate ( Betamethasone Sodium Phosphate And Betamethasone Acetate )

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NDC Code : 76420-007-05 – JSON Data Format

                
{
  "NDC": {
    "NDCCode": "76420-007-05",
    "PackageDescription": "5 mL in 1 VIAL, MULTI-DOSE (76420-007-05) ",
    "NDC11Code": "76420-0007-05",
    "ProductNDC": "76420-007",
    "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
    "ProprietaryName": "Betamethasone Sodium Phosphate And Betamethasone Acetate",
    "ProprietaryNameSuffix": null,
    "NonProprietaryName": "Betamethasone Sodium Phosphate And Betamethasone Acetate",
    "DosageFormName": "INJECTION, SUSPENSION",
    "RouteName": "INTRA-ARTICULAR; INTRALESIONAL; INTRAMUSCULAR",
    "StartMarketingDate": "20100428",
    "EndMarketingDate": null,
    "MarketingCategoryName": "ANDA",
    "ApplicationNumber": "ANDA090747",
    "LabelerName": "Asclemed USA, Inc.",
    "SubstanceName": "BETAMETHASONE ACETATE; BETAMETHASONE SODIUM PHOSPHATE",
    "StrengthNumber": "3; 3",
    "StrengthUnit": "mg/mL; mg/mL",
    "Pharm_Classes": "Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid Hormone Receptor Agonists [MoA], Corticosteroid [EPC], Corticosteroid [EPC]",
    "DEASchedule": null,
    "Status": "Active",
    "LastUpdate": "2022-10-13",
    "PackageNdcExcludeFlag": "N",
    "ProductNdcExcludeFlag": "N",
    "ListingRecordCertifiedThrough": "20261231",
    "StartMarketingDatePackage": "20200116",
    "EndMarketingDatePackage": null,
    "SamplePackage": "N"
  }
}