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    NDC 70518-1385-02 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 REMEDYREPACK INC.. The primary component is VENLAFAXINE HYDROCHLORIDE.

    Product Information

    NDC 70518-1385
    Product ID 70518-1385_09a6f385-0a8b-d55e-e063-6394a90a5e55
    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 REMEDYREPACK INC.
    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 70518-1385-02 (70518138502)

    NDC Package Code 70518-1385-2
    Billing NDC 70518138502
    Package 30 TABLET in 1 BOTTLE, PLASTIC (70518-1385-2)
    Marketing Start Date 2021-02-01
    NDC Exclude Flag N
    Pricing Information N/A