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    NDC 55154-1341-00 Fluoxetine 20 mg/1 Details

    Fluoxetine 20 mg/1

    Fluoxetine is a ORAL CAPSULE in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Cardinal Health 107, LLC. The primary component is FLUOXETINE HYDROCHLORIDE.

    Product Information

    NDC 55154-1341
    Product ID 55154-1341_1c737dbb-c86a-47ec-b433-a59d46ff121f
    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 Fluoxetine
    Proprietary Name Suffix n/a
    Non-Proprietary Name Fluoxetine
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form CAPSULE
    Route ORAL
    Active Ingredient Strength 20
    Active Ingredient Units mg/1
    Substance Name FLUOXETINE HYDROCHLORIDE
    Labeler Name Cardinal Health 107, LLC
    Pharmaceutical Class Serotonin Reuptake Inhibitor [EPC], Serotonin Uptake Inhibitors [MoA]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA076001
    Listing Certified Through 2024-12-31

    Package

    NDC 55154-1341-00 (55154134100)

    NDC Package Code 55154-1341-0
    Billing NDC 55154134100
    Package 10 BLISTER PACK in 1 BAG (55154-1341-0) / 1 CAPSULE in 1 BLISTER PACK
    Marketing Start Date 2007-02-16
    NDC Exclude Flag N
    Pricing Information N/A