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    NDC 71335-1753-03 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 Bryant Ranch Prepack. The primary component is DESVENLAFAXINE SUCCINATE.

    Product Information

    NDC 71335-1753
    Product ID 71335-1753_57b9bd7c-6404-4667-89a1-bc2c29fa789b
    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 Desvenlafaxine
    Proprietary Name Suffix n/a
    Non-Proprietary Name Desvenlafaxine
    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 Bryant Ranch Prepack
    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 ANDA210014
    Listing Certified Through 2024-12-31

    Package

    NDC 71335-1753-03 (71335175303)

    NDC Package Code 71335-1753-3
    Billing NDC 71335175303
    Package 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1753-3)
    Marketing Start Date 2022-07-01
    NDC Exclude Flag N
    Pricing Information N/A