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    NDC 51655-0323-52 venlafaxine 37.5 mg/1 Details

    venlafaxine 37.5 mg/1

    venlafaxine is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Northwind Pharmaceuticals, LLC. The primary component is VENLAFAXINE HYDROCHLORIDE.

    Product Information

    NDC 51655-0323
    Product ID 51655-323_fb0764e5-d66e-fe80-e053-6394a90ae782
    Associated GPIs
    GCN Sequence Number n/a
    GCN Sequence Number Description n/a
    HIC3 n/a
    HIC3 Description n/a
    GCN n/a
    HICL Sequence Number n/a
    HICL Sequence Number Description n/a
    Brand/Generic n/a
    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 37.5
    Active Ingredient Units mg/1
    Substance Name VENLAFAXINE HYDROCHLORIDE
    Labeler Name Northwind Pharmaceuticals, LLC
    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 51655-0323-52 (51655032352)

    NDC Package Code 51655-323-52
    Billing NDC 51655032352
    Package 30 TABLET in 1 BOTTLE, PLASTIC (51655-323-52)
    Marketing Start Date 2023-05-02
    NDC Exclude Flag N
    Pricing Information N/A