82009-056-10 : NDC 2026 Code

82009-056-10 : Venlafaxine Hydrochloride ( Venlafaxine Hydrochloride )

Additionally :

You can get information about “82009-056-10” NDC code in 82009-056-10 in HTML format

HTML | 82009-056-10 in TXT (Plain Text) format

TXT | 82009-056-10 in PDF (Portable Document Format)

PDF | 82009-056-10 in XML format

XML formats.

NDC Code : 82009-056-10 – JSON Data Format

                
{
  "NDC": {
    "NDCCode": "82009-056-10",
    "PackageDescription": "1000 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (82009-056-10) ",
    "NDC11Code": "82009-0056-10",
    "ProductNDC": "82009-056",
    "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
    "ProprietaryName": "Venlafaxine Hydrochloride",
    "ProprietaryNameSuffix": null,
    "NonProprietaryName": "Venlafaxine Hydrochloride",
    "DosageFormName": "CAPSULE, EXTENDED RELEASE",
    "RouteName": "ORAL",
    "StartMarketingDate": "20221121",
    "EndMarketingDate": null,
    "MarketingCategoryName": "ANDA",
    "ApplicationNumber": "ANDA200834",
    "LabelerName": "QUALLENT PHARMACEUTICALS HEALTH LLC",
    "SubstanceName": "VENLAFAXINE HYDROCHLORIDE",
    "StrengthNumber": "37.5",
    "StrengthUnit": "mg/1",
    "Pharm_Classes": "Norepinephrine Uptake Inhibitors [MoA], Serotonin Uptake Inhibitors [MoA], Serotonin and Norepinephrine Reuptake Inhibitor [EPC]",
    "DEASchedule": null,
    "Status": "Active",
    "LastUpdate": "2024-06-11",
    "PackageNdcExcludeFlag": "N",
    "ProductNdcExcludeFlag": "N",
    "ListingRecordCertifiedThrough": "20261231",
    "StartMarketingDatePackage": "20221121",
    "EndMarketingDatePackage": null,
    "SamplePackage": "N"
  }
}