41616-760-18 : NDC 2026 Code

41616-760-18 : Venlafaxine Hydrochloride ( Venlafaxine Hydrochloride )

Additionally :

You can get information about “41616-760-18” NDC code in 41616-760-18 in HTML format

HTML | 41616-760-18 in TXT (Plain Text) format

TXT | 41616-760-18 in PDF (Portable Document Format)

PDF | 41616-760-18 in XML format

XML formats.

NDC Code : 41616-760-18 – JSON Data Format

                
{
  "NDC": {
    "NDCCode": "41616-760-18",
    "PackageDescription": "1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (41616-760-18)",
    "NDC11Code": "41616-0760-18",
    "ProductNDC": "41616-760",
    "ProductTypeName": "HUMAN PRESCRIPTION DRUG",
    "ProprietaryName": "Venlafaxine Hydrochloride",
    "ProprietaryNameSuffix": null,
    "NonProprietaryName": "Venlafaxine Hydrochloride",
    "DosageFormName": "TABLET, EXTENDED RELEASE",
    "RouteName": "ORAL",
    "StartMarketingDate": "20100818",
    "EndMarketingDate": null,
    "MarketingCategoryName": "ANDA",
    "ApplicationNumber": "ANDA091272",
    "LabelerName": "Sun Pharma Global Inc.",
    "SubstanceName": "VENLAFAXINE HYDROCHLORIDE",
    "StrengthNumber": "37.5",
    "StrengthUnit": "mg/1",
    "Pharm_Classes": "Norepinephrine Uptake Inhibitors [MoA],Serotonin and Norepinephrine Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA]",
    "DEASchedule": null,
    "Status": "Deprecated",
    "LastUpdate": "2017-09-07",
    "PackageNdcExcludeFlag": null,
    "ProductNdcExcludeFlag": null,
    "ListingRecordCertifiedThrough": null,
    "StartMarketingDatePackage": null,
    "EndMarketingDatePackage": null,
    "SamplePackage": null
  }
}