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    NDC 62175-0472-41 Paroxetine Hydrochloride 37.5 mg/1 Details

    Paroxetine Hydrochloride 37.5 mg/1

    Paroxetine Hydrochloride is a ORAL TABLET, FILM COATED, EXTENDED RELEASE in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Lannett Company, Inc.. The primary component is PAROXETINE HYDROCHLORIDE.

    Product Information

    NDC 62175-0472
    Product ID 62175-472_9474f942-d6d8-486b-8ea6-f8c561bb5014
    Associated GPIs 58160060007540
    GCN Sequence Number 050138
    GCN Sequence Number Description paroxetine HCl TAB ER 24H 37.5 MG ORAL
    HIC3 H2S
    HIC3 Description SELECTIVE SEROTONIN REUPTAKE INHIBITOR (SSRIS)
    GCN 17079
    HICL Sequence Number 007344
    HICL Sequence Number Description PAROXETINE HCL
    Brand/Generic Generic
    Proprietary Name Paroxetine Hydrochloride
    Proprietary Name Suffix n/a
    Non-Proprietary Name Paroxetine Hydrochloride
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET, FILM COATED, EXTENDED RELEASE
    Route ORAL
    Active Ingredient Strength 37.5
    Active Ingredient Units mg/1
    Substance Name PAROXETINE HYDROCHLORIDE
    Labeler Name Lannett Company, Inc.
    Pharmaceutical Class Serotonin Reuptake Inhibitor [EPC], Serotonin Uptake Inhibitors [MoA]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA204744
    Listing Certified Through 2024-12-31

    Package

    NDC 62175-0472-41 (62175047241)

    NDC Package Code 62175-472-41
    Billing NDC 62175047241
    Package 500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (62175-472-41)
    Marketing Start Date 2014-10-31
    NDC Exclude Flag N
    Pricing Information N/A