71839-121-25 : NDC 2026 Code

71839-121-25 : Succinylcholine Chloride ( Succinylcholine Chloride )

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NDC Code : 71839-121-25 – JSON Data Format

                
{
  "NDC": {
    "NDCCode": "71839-121-25",
    "PackageDescription": "25 VIAL, MULTI-DOSE in 1 CARTON (71839-121-25)  / 10 mL in 1 VIAL, MULTI-DOSE (71839-121-01) ",
    "NDC11Code": "71839-0121-25",
    "ProductNDC": "71839-121",
    "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
    "ProprietaryName": "Succinylcholine Chloride",
    "ProprietaryNameSuffix": null,
    "NonProprietaryName": "Succinylcholine Chloride",
    "DosageFormName": "INJECTION, SOLUTION",
    "RouteName": "INTRAMUSCULAR; INTRAVENOUS",
    "StartMarketingDate": "20220207",
    "EndMarketingDate": null,
    "MarketingCategoryName": "ANDA",
    "ApplicationNumber": "ANDA216003",
    "LabelerName": "BE Pharmaceuticals Inc.",
    "SubstanceName": "SUCCINYLCHOLINE CHLORIDE",
    "StrengthNumber": "20",
    "StrengthUnit": "mg/mL",
    "Pharm_Classes": "Depolarizing Neuromuscular Blocker [EPC], Neuromuscular Depolarizing Blockade [PE]",
    "DEASchedule": null,
    "Status": "Active",
    "LastUpdate": "2023-12-21",
    "PackageNdcExcludeFlag": "N",
    "ProductNdcExcludeFlag": "N",
    "ListingRecordCertifiedThrough": "20261231",
    "StartMarketingDatePackage": "20220207",
    "EndMarketingDatePackage": null,
    "SamplePackage": "N"
  }
}