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    NDC 17224-0171-21 Fluoxetine 10 mg/1 Details

    Fluoxetine 10 mg/1

    Fluoxetine is a ORAL CAPSULE in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Calvin Scott & Co., Inc.. The primary component is FLUOXETINE HYDROCHLORIDE.

    Product Information

    NDC 17224-0171
    Product ID 17224-171_f709b80f-6425-790e-e053-6394a90a17fc
    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 HYDROCHLORIDE
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form CAPSULE
    Route ORAL
    Active Ingredient Strength 10
    Active Ingredient Units mg/1
    Substance Name FLUOXETINE HYDROCHLORIDE
    Labeler Name Calvin Scott & Co., Inc.
    Pharmaceutical Class Serotonin Reuptake Inhibitor [EPC], Serotonin Uptake Inhibitors [MoA]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA204597
    Listing Certified Through 2024-12-31

    Package

    NDC 17224-0171-21 (17224017121)

    NDC Package Code 17224-171-21
    Billing NDC 17224017121
    Package 21 CAPSULE in 1 BOTTLE (17224-171-21)
    Marketing Start Date 2015-03-16
    NDC Exclude Flag N
    Pricing Information N/A