16714-852-01 : NDC 2026 Code

16714-852-01 : Metoprolol Succinate ( Metoprolol Succinate )

Additionally :

You can get information about “16714-852-01” NDC code in 16714-852-01 in HTML format

HTML | 16714-852-01 in TXT (Plain Text) format

TXT | 16714-852-01 in PDF (Portable Document Format)

PDF | 16714-852-01 in XML format

XML formats.

NDC Code : 16714-852-01 – JSON Data Format

                
{
  "NDC": {
    "NDCCode": "16714-852-01",
    "PackageDescription": "100 TABLET, EXTENDED RELEASE in 1 BOTTLE (16714-852-01) ",
    "NDC11Code": "16714-0852-01",
    "ProductNDC": "16714-852",
    "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
    "ProprietaryName": "Metoprolol Succinate",
    "ProprietaryNameSuffix": null,
    "NonProprietaryName": "Metoprolol Succinate",
    "DosageFormName": "TABLET, EXTENDED RELEASE",
    "RouteName": "ORAL",
    "StartMarketingDate": "20180827",
    "EndMarketingDate": "20250731",
    "MarketingCategoryName": "ANDA",
    "ApplicationNumber": "ANDA203894",
    "LabelerName": "Northstar Rx LLC",
    "SubstanceName": "METOPROLOL SUCCINATE",
    "StrengthNumber": "25",
    "StrengthUnit": "mg/1",
    "Pharm_Classes": "Adrenergic beta-Antagonists [MoA], beta-Adrenergic Blocker [EPC]",
    "DEASchedule": null,
    "Status": "Deprecated",
    "LastUpdate": "2025-08-02",
    "PackageNdcExcludeFlag": "N",
    "ProductNdcExcludeFlag": "N",
    "ListingRecordCertifiedThrough": null,
    "StartMarketingDatePackage": "20180827",
    "EndMarketingDatePackage": "20250731",
    "SamplePackage": "N"
  }
}