36000-336-25 : NDC 2026 Code

36000-336-25 : Ephedrine Sulfate ( Ephedrine Sulfate )

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NDC Code : 36000-336-25 – JSON Data Format

                
{
  "NDC": {
    "NDCCode": "36000-336-25",
    "PackageDescription": "25 VIAL, SINGLE-DOSE in 1 CARTON (36000-336-25)  / 1 mL in 1 VIAL, SINGLE-DOSE (36000-336-01) ",
    "NDC11Code": "36000-0336-25",
    "ProductNDC": "36000-336",
    "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
    "ProprietaryName": "Ephedrine Sulfate",
    "ProprietaryNameSuffix": null,
    "NonProprietaryName": "Ephedrine Sulfate",
    "DosageFormName": "INJECTION",
    "RouteName": "INTRAVENOUS",
    "StartMarketingDate": "20260708",
    "EndMarketingDate": null,
    "MarketingCategoryName": "ANDA",
    "ApplicationNumber": "ANDA216740",
    "LabelerName": "Baxter Healthcare Corporation",
    "SubstanceName": "EPHEDRINE SULFATE",
    "StrengthNumber": "50",
    "StrengthUnit": "mg/mL",
    "Pharm_Classes": "Adrenergic alpha-Agonists [MoA], Adrenergic beta-Agonists [MoA], Increased Norepinephrine Activity [PE], Norepinephrine Releasing Agent [EPC], alpha-Adrenergic Agonist [EPC], beta-Adrenergic Agonist [EPC]",
    "DEASchedule": null,
    "Status": "Active",
    "LastUpdate": "2026-07-17",
    "PackageNdcExcludeFlag": "N",
    "ProductNdcExcludeFlag": "N",
    "ListingRecordCertifiedThrough": "20271231",
    "StartMarketingDatePackage": "20260708",
    "EndMarketingDatePackage": null,
    "SamplePackage": "N"
  }
}