68071-1856-1 : NDC 2026 Code

68071-1856-1 : Propranolol Hydrochloride ( Propranolol Hydrochloride )

Additionally :

You can get information about “68071-1856-1” NDC code in 68071-1856-1 in HTML format

HTML | 68071-1856-1 in TXT (Plain Text) format

TXT | 68071-1856-1 in PDF (Portable Document Format)

PDF | 68071-1856-1 in XML format

XML formats.

NDC Code : 68071-1856-1 – JSON Data Format

                
{
  "NDC": {
    "NDCCode": "68071-1856-1",
    "PackageDescription": "100 TABLET in 1 BOTTLE (68071-1856-1)",
    "NDC11Code": "68071-1856-01",
    "ProductNDC": "68071-1856",
    "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
    "ProprietaryName": "Propranolol Hydrochloride",
    "ProprietaryNameSuffix": null,
    "NonProprietaryName": "Propranolol Hydrochloride",
    "DosageFormName": "TABLET",
    "RouteName": "ORAL",
    "StartMarketingDate": "20100621",
    "EndMarketingDate": null,
    "MarketingCategoryName": "ANDA",
    "ApplicationNumber": "ANDA070219",
    "LabelerName": "NuCare Pharmceuticals,Inc.",
    "SubstanceName": "PROPRANOLOL HYDROCHLORIDE",
    "StrengthNumber": "40",
    "StrengthUnit": "mg/1",
    "Pharm_Classes": "Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC]",
    "DEASchedule": null,
    "Status": "Deprecated",
    "LastUpdate": "2020-04-18",
    "PackageNdcExcludeFlag": null,
    "ProductNdcExcludeFlag": "N",
    "ListingRecordCertifiedThrough": "20201231",
    "StartMarketingDatePackage": null,
    "EndMarketingDatePackage": null,
    "SamplePackage": null
  }
}