0121-2106-02 : NDC 2026 Code

0121-2106-02 : Leuprolide Acetate ( Leuprolide Acetate )

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NDC Code : 0121-2106-02 – JSON Data Format

                
{
  "NDC": {
    "NDCCode": "0121-2106-02",
    "PackageDescription": "1 KIT in 1 CARTON (0121-2106-02)  *  1 VIAL, MULTI-DOSE in 1 CARTON (0121-1053-02)  / 2.8 mL in 1 VIAL, MULTI-DOSE *  1 mL in 1 PACKET (0121-2105-01) ",
    "NDC11Code": "00121-2106-02",
    "ProductNDC": "0121-2106",
    "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
    "ProprietaryName": "Leuprolide Acetate",
    "ProprietaryNameSuffix": null,
    "NonProprietaryName": "Leuprolide Acetate",
    "DosageFormName": "KIT",
    "RouteName": "SUBCUTANEOUS",
    "StartMarketingDate": "20250201",
    "EndMarketingDate": null,
    "MarketingCategoryName": "ANDA",
    "ApplicationNumber": "ANDA217957",
    "LabelerName": "PAI Holdings, LLC dba PAI Pharma",
    "SubstanceName": null,
    "StrengthNumber": null,
    "StrengthUnit": null,
    "Pharm_Classes": null,
    "DEASchedule": null,
    "Status": "Active",
    "LastUpdate": "2025-02-04",
    "PackageNdcExcludeFlag": "N",
    "ProductNdcExcludeFlag": "N",
    "ListingRecordCertifiedThrough": "20261231",
    "StartMarketingDatePackage": "20250201",
    "EndMarketingDatePackage": null,
    "SamplePackage": "N"
  }
}