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    NDC 70518-1253-01 Paroxetine 40 mg/1 Details

    Paroxetine 40 mg/1

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

    Product Information

    NDC 70518-1253
    Product ID 70518-1253_f93a697c-e39f-8f4b-e053-6294a90a2c77
    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 Paroxetine
    Proprietary Name Suffix n/a
    Non-Proprietary Name paroxetine hydrochloride hemihydrate
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET, FILM COATED
    Route ORAL
    Active Ingredient Strength 40
    Active Ingredient Units mg/1
    Substance Name PAROXETINE HYDROCHLORIDE HEMIHYDRATE
    Labeler Name REMEDYREPACK INC.
    Pharmaceutical Class Serotonin Reuptake Inhibitor [EPC], Serotonin Uptake Inhibitors [MoA]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA203854
    Listing Certified Through 2024-12-31

    Package

    NDC 70518-1253-01 (70518125301)

    NDC Package Code 70518-1253-1
    Billing NDC 70518125301
    Package 30 POUCH in 1 BOX (70518-1253-1) / 1 TABLET, FILM COATED in 1 POUCH (70518-1253-2)
    Marketing Start Date 2022-01-14
    NDC Exclude Flag N
    Pricing Information N/A