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51662-1338-3 : NDC 2026 Code

51662-1338-3 : Propranolol Hydrochloride ( Propranolol Hydrochloride )

Additionally :
You can get information about “51662-1338-3” NDC code in 51662-1338-3 in HTML format HTML  |  51662-1338-3 in TXT (Plain Text) format TXT  |  51662-1338-3 in PDF (Portable Document Format) PDF  |  51662-1338-3 in XML format XML  formats.

NDC Code : 51662-1338-3 – JSON Data Format

                
{
  "NDC": {
    "NDCCode": "51662-1338-3",
    "PackageDescription": "10 POUCH in 1 CASE (51662-1338-3)  / 1 VIAL in 1 POUCH (51662-1338-2)  / 1 mL in 1 VIAL",
    "NDC11Code": "51662-1338-03",
    "ProductNDC": "51662-1338",
    "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
    "ProprietaryName": "Propranolol Hydrochloride",
    "ProprietaryNameSuffix": null,
    "NonProprietaryName": "Propranolol Hydrochloride",
    "DosageFormName": "INJECTION",
    "RouteName": "INTRAVENOUS",
    "StartMarketingDate": "20181222",
    "EndMarketingDate": null,
    "MarketingCategoryName": "ANDA",
    "ApplicationNumber": "ANDA077760",
    "LabelerName": "HF Acquisition Co LLC, DBA HealthFirst",
    "SubstanceName": "PROPRANOLOL HYDROCHLORIDE",
    "StrengthNumber": "1",
    "StrengthUnit": "mg/mL",
    "Pharm_Classes": "Adrenergic beta-Antagonists [MoA], beta-Adrenergic Blocker [EPC]",
    "DEASchedule": null,
    "Status": "Active",
    "LastUpdate": "2025-06-18",
    "PackageNdcExcludeFlag": "N",
    "ProductNdcExcludeFlag": "N",
    "ListingRecordCertifiedThrough": "20261231",
    "StartMarketingDatePackage": "20221001",
    "EndMarketingDatePackage": null,
    "SamplePackage": "N"
  }
}
                
            

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