60687-313-25 : NDC 2026 Code

60687-313-25 : Nadolol ( Nadolol )

Additionally :

You can get information about “60687-313-25” NDC code in 60687-313-25 in HTML format

HTML | 60687-313-25 in TXT (Plain Text) format

TXT | 60687-313-25 in PDF (Portable Document Format)

PDF | 60687-313-25 in XML format

XML formats.

NDC Code : 60687-313-25 – JSON Data Format

                
{
  "NDC": {
    "NDCCode": "60687-313-25",
    "PackageDescription": "30 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-313-25)  / 1 TABLET in 1 BLISTER PACK (60687-313-95) ",
    "NDC11Code": "60687-0313-25",
    "ProductNDC": "60687-313",
    "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
    "ProprietaryName": "Nadolol",
    "ProprietaryNameSuffix": null,
    "NonProprietaryName": "Nadolol",
    "DosageFormName": "TABLET",
    "RouteName": "ORAL",
    "StartMarketingDate": "20170613",
    "EndMarketingDate": "20251231",
    "MarketingCategoryName": "ANDA",
    "ApplicationNumber": "ANDA203455",
    "LabelerName": "American Health Packaging",
    "SubstanceName": "NADOLOL",
    "StrengthNumber": "40",
    "StrengthUnit": "mg/1",
    "Pharm_Classes": "Adrenergic beta-Antagonists [MoA], beta-Adrenergic Blocker [EPC]",
    "DEASchedule": null,
    "Status": "Deprecated",
    "LastUpdate": "2026-01-01",
    "PackageNdcExcludeFlag": "N",
    "ProductNdcExcludeFlag": "N",
    "ListingRecordCertifiedThrough": null,
    "StartMarketingDatePackage": "20170613",
    "EndMarketingDatePackage": "20251231",
    "SamplePackage": "N"
  }
}