Search by Drug Name or NDC

    NDC 51655-0717-52 venlafaxine 100 mg/1 Details

    venlafaxine 100 mg/1

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

    Product Information

    NDC 51655-0717
    Product ID 51655-717_db5f1693-ca65-7a97-e053-2995a90acbff
    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 100
    Active Ingredient Units mg/1
    Substance Name VENLAFAXINE HYDROCHLORIDE
    Labeler Name Northwind Pharmaceuticals
    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 ANDA078932
    Listing Certified Through 2024-12-31

    Package

    NDC 51655-0717-52 (51655071752)

    NDC Package Code 51655-717-52
    Billing NDC 51655071752
    Package 30 TABLET in 1 BOTTLE, PLASTIC (51655-717-52)
    Marketing Start Date 2021-05-26
    NDC Exclude Flag N
    Pricing Information N/A