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    NDC 65862-0407-30 Venlafaxine 75 mg/1 Details

    Venlafaxine 75 mg/1

    Venlafaxine is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Aurobindo Pharma Limited. The primary component is VENLAFAXINE HYDROCHLORIDE.

    Product Information

    NDC 65862-0407
    Product ID 65862-407_426d12db-50e2-4915-999f-84645fb387d9
    Associated GPIs 58180090100360
    GCN Sequence Number 046401
    GCN Sequence Number Description venlafaxine HCl TABLET 75 MG ORAL
    HIC3 H7C
    HIC3 Description SEROTONIN-NOREPINEPHRINE REUPTAKE-INHIB (SNRIS)
    GCN 16814
    HICL Sequence Number 008847
    HICL Sequence Number Description VENLAFAXINE HCL
    Brand/Generic Generic
    Proprietary Name Venlafaxine
    Proprietary Name Suffix n/a
    Non-Proprietary Name Venlafaxine Hydrochloride
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET
    Route ORAL
    Active Ingredient Strength 75
    Active Ingredient Units mg/1
    Substance Name VENLAFAXINE HYDROCHLORIDE
    Labeler Name Aurobindo Pharma Limited
    Pharmaceutical Class Norepinephrine Uptake Inhibitors [MoA], Serotonin Uptake Inhibitors [MoA], Serotonin and Norepinephrine Reuptake Inhibitor [EPC]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA090555
    Listing Certified Through 2024-12-31

    Package

    NDC 65862-0407-30 (65862040730)

    NDC Package Code 65862-407-30
    Billing NDC 65862040730
    Package 30 TABLET in 1 BOTTLE (65862-407-30)
    Marketing Start Date 2010-04-07
    NDC Exclude Flag N
    Pricing Information N/A