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    NDC 70518-3322-00 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 REMEDYREPACK INC.. The primary component is FLUOXETINE HYDROCHLORIDE.

    Product Information

    NDC 70518-3322
    Product ID 70518-3322_06c07eb6-83a2-38b9-e063-6294a90ade6b
    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 20
    Active Ingredient Units mg/1
    Substance Name FLUOXETINE HYDROCHLORIDE
    Labeler Name REMEDYREPACK 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 70518-3322-00 (70518332200)

    NDC Package Code 70518-3322-0
    Billing NDC 70518332200
    Package 30 CAPSULE in 1 BLISTER PACK (70518-3322-0)
    Marketing Start Date 2021-12-29
    NDC Exclude Flag N
    Pricing Information N/A