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    NDC 61919-0322-30 PAROXETINE 10 mg/1 Details

    PAROXETINE 10 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 ANHYDROUS.

    Product Information

    NDC 61919-0322
    Product ID 61919-322_fb594428-cc55-6afa-e053-6394a90ab152
    Associated GPIs 58160060000310
    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 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 10
    Active Ingredient Units mg/1
    Substance Name PAROXETINE HYDROCHLORIDE ANHYDROUS
    Labeler Name DIRECT RX
    Pharmaceutical Class Serotonin Reuptake Inhibitor [EPC], Serotonin Uptake Inhibitors [MoA]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA075356
    Listing Certified Through 2024-12-31

    Package

    NDC 61919-0322-30 (61919032230)

    NDC Package Code 61919-322-30
    Billing NDC 61919032230
    Package 30 TABLET, FILM COATED in 1 BOTTLE (61919-322-30)
    Marketing Start Date 2015-01-01
    NDC Exclude Flag N
    Pricing Information N/A