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    NDC 70518-1547-00 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 REMEDYREPACK INC.. The primary component is VENLAFAXINE HYDROCHLORIDE.

    Product Information

    NDC 70518-1547
    Product ID 70518-1547_0a967fbc-538c-7fd7-e063-6294a90a7db0
    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
    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 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 ANDA078627
    Listing Certified Through 2024-12-31

    Package

    NDC 70518-1547-00 (70518154700)

    NDC Package Code 70518-1547-0
    Billing NDC 70518154700
    Package 30 TABLET in 1 BLISTER PACK (70518-1547-0)
    Marketing Start Date 2018-10-17
    NDC Exclude Flag N
    Pricing Information N/A