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    NDC 70518-2448-04 Sertraline Hydrochloride 100 mg/1 Details

    Sertraline Hydrochloride 100 mg/1

    Sertraline Hydrochloride is a ORAL TABLET, FILM COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by REMEDYREPACK INC.. The primary component is SERTRALINE HYDROCHLORIDE.

    Product Information

    NDC 70518-2448
    Product ID 70518-2448_0b4e90dd-642b-afec-e063-6294a90a598e
    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 Sertraline Hydrochloride
    Proprietary Name Suffix n/a
    Non-Proprietary Name Sertraline Hydrochloride
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET, FILM COATED
    Route ORAL
    Active Ingredient Strength 100
    Active Ingredient Units mg/1
    Substance Name SERTRALINE HYDROCHLORIDE
    Labeler Name REMEDYREPACK INC.
    Pharmaceutical Class Cytochrome P450 2D6 Inhibitors [MoA], Serotonin Reuptake Inhibitor [EPC], Serotonin Uptake Inhibitors [MoA]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA077206
    Listing Certified Through 2024-12-31

    Package

    NDC 70518-2448-04 (70518244804)

    NDC Package Code 70518-2448-4
    Billing NDC 70518244804
    Package 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-2448-4)
    Marketing Start Date 2020-12-22
    NDC Exclude Flag N
    Pricing Information N/A