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    NDC 68788-7194-06 Desvenlafaxine 50 mg/1 Details

    Desvenlafaxine 50 mg/1

    Desvenlafaxine is a ORAL TABLET, EXTENDED RELEASE in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Preferred Pharmaceutical, Inc.. The primary component is DESVENLAFAXINE SUCCINATE.

    Product Information

    NDC 68788-7194
    Product ID 68788-7194_25478037-08dc-452a-9499-732032a1fd9f
    Associated GPIs 58180020207520
    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 Desvenlafaxine
    Proprietary Name Suffix n/a
    Non-Proprietary Name Desvenlafaxine Succinate
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET, EXTENDED RELEASE
    Route ORAL
    Active Ingredient Strength 50
    Active Ingredient Units mg/1
    Substance Name DESVENLAFAXINE SUCCINATE
    Labeler Name Preferred Pharmaceutical, Inc.
    Pharmaceutical Class Cytochrome P450 2D6 Inhibitors [MoA], Norepinephrine Uptake Inhibitors [MoA], Serotonin Uptake Inhibitors [MoA], Serotonin and Norepinephrine Reuptake Inhibitor [EPC]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA204003
    Listing Certified Through 2024-12-31

    Package

    NDC 68788-7194-06 (68788719406)

    NDC Package Code 68788-7194-6
    Billing NDC 68788719406
    Package 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-7194-6)
    Marketing Start Date 2018-07-18
    NDC Exclude Flag N
    Pricing Information N/A