51407-709-01 : NDC 2026 Code

51407-709-01 : Ramipril ( Ramipril )

Additionally :

You can get information about “51407-709-01” NDC code in 51407-709-01 in HTML format

HTML | 51407-709-01 in TXT (Plain Text) format

TXT | 51407-709-01 in PDF (Portable Document Format)

PDF | 51407-709-01 in XML format

XML formats.

NDC Code : 51407-709-01 – JSON Data Format

                
{
  "NDC": {
    "NDCCode": "51407-709-01",
    "PackageDescription": "100 CAPSULE in 1 BOTTLE (51407-709-01) ",
    "NDC11Code": "51407-0709-01",
    "ProductNDC": "51407-709",
    "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
    "ProprietaryName": "Ramipril",
    "ProprietaryNameSuffix": null,
    "NonProprietaryName": "Ramipril",
    "DosageFormName": "CAPSULE",
    "RouteName": "ORAL",
    "StartMarketingDate": "20250708",
    "EndMarketingDate": null,
    "MarketingCategoryName": "ANDA",
    "ApplicationNumber": "ANDA079116",
    "LabelerName": "GSMS, Incorporated",
    "SubstanceName": "RAMIPRIL",
    "StrengthNumber": "10",
    "StrengthUnit": "mg/1",
    "Pharm_Classes": "Angiotensin Converting Enzyme Inhibitor [EPC], Angiotensin-converting Enzyme Inhibitors [MoA]",
    "DEASchedule": null,
    "Status": "Active",
    "LastUpdate": "2025-07-12",
    "PackageNdcExcludeFlag": "N",
    "ProductNdcExcludeFlag": "N",
    "ListingRecordCertifiedThrough": "20261231",
    "StartMarketingDatePackage": "20250708",
    "EndMarketingDatePackage": null,
    "SamplePackage": "N"
  }
}