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    NDC 42571-0387-10 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 Micro Labs Limited. The primary component is FLUOXETINE HYDROCHLORIDE.

    Product Information

    NDC 42571-0387
    Product ID 42571-387_0770266d-0043-f296-e063-6294a90a1d1c
    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 10
    Active Ingredient Units mg/1
    Substance Name FLUOXETINE HYDROCHLORIDE
    Labeler Name Micro Labs Limited
    Pharmaceutical Class Serotonin Reuptake Inhibitor [EPC], Serotonin Uptake Inhibitors [MoA]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA216232
    Listing Certified Through 2024-12-31

    Package

    NDC 42571-0387-10 (42571038710)

    NDC Package Code 42571-387-10
    Billing NDC 42571038710
    Package 1000 CAPSULE in 1 BOTTLE (42571-387-10)
    Marketing Start Date 2023-01-01
    NDC Exclude Flag N
    Pricing Information N/A
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