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    NDC 70518-1406-00 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 REMEDYREPACK INC.. The primary component is PAROXETINE HYDROCHLORIDE HEMIHYDRATE.

    Product Information

    NDC 70518-1406
    Product ID 70518-1406_0a4a0161-4b6e-c0b4-e063-6394a90a801f
    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 10
    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 70518-1406-00 (70518140600)

    NDC Package Code 70518-1406-0
    Billing NDC 70518140600
    Package 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-1406-0)
    Marketing Start Date 2018-09-07
    NDC Exclude Flag N
    Pricing Information N/A