Search by Drug Name or NDC

    NDC 61919-0658-30 PAROXETINE 20 mg/1 Details

    PAROXETINE 20 mg/1

    PAROXETINE is a ORAL TABLET, FILM COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by DIRECT RX. The primary component is PAROXETINE HYDROCHLORIDE HEMIHYDRATE.

    Product Information

    NDC 61919-0658
    Product ID 61919-658_fb594428-cc55-6afa-e053-6394a90ab152
    Associated GPIs 58160060000320
    GCN Sequence Number 046223
    GCN Sequence Number Description paroxetine HCl TABLET 20 MG ORAL
    HIC3 H2S
    HIC3 Description SELECTIVE SEROTONIN REUPTAKE INHIBITOR (SSRIS)
    GCN 16366
    HICL Sequence Number 007344
    HICL Sequence Number Description PAROXETINE HCL
    Brand/Generic Generic
    Proprietary Name PAROXETINE
    Proprietary Name Suffix n/a
    Non-Proprietary Name PAROXETINE
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET, FILM COATED
    Route ORAL
    Active Ingredient Strength 20
    Active Ingredient Units mg/1
    Substance Name PAROXETINE HYDROCHLORIDE HEMIHYDRATE
    Labeler Name DIRECT RX
    Pharmaceutical Class Serotonin Reuptake Inhibitor [EPC], Serotonin Uptake Inhibitors [MoA]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA077584
    Listing Certified Through 2024-12-31

    Package

    NDC 61919-0658-30 (61919065830)

    NDC Package Code 61919-658-30
    Billing NDC 61919065830
    Package 30 TABLET, FILM COATED in 1 BOTTLE (61919-658-30)
    Marketing Start Date 2019-04-19
    NDC Exclude Flag N
    Pricing Information N/A