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    NDC 71335-1882-04 PAROXETINE HYDROCHLORIDE 25 mg/1 Details

    PAROXETINE HYDROCHLORIDE 25 mg/1

    PAROXETINE HYDROCHLORIDE is a ORAL TABLET, FILM COATED, EXTENDED RELEASE in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Bryant Ranch Prepack. The primary component is PAROXETINE HYDROCHLORIDE HEMIHYDRATE.

    Product Information

    NDC 71335-1882
    Product ID 71335-1882_33af74d2-0303-4513-b99e-def945a94981
    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 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 25
    Active Ingredient Units mg/1
    Substance Name PAROXETINE HYDROCHLORIDE HEMIHYDRATE
    Labeler Name Bryant Ranch Prepack
    Pharmaceutical Class Serotonin Reuptake Inhibitor [EPC], Serotonin Uptake Inhibitors [MoA]
    DEA Schedule n/a
    Marketing Category NDA
    Application Number NDA020936
    Listing Certified Through 2023-12-31

    Package

    NDC 71335-1882-04 (71335188204)

    NDC Package Code 71335-1882-4
    Billing NDC 71335188204
    Package 110 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-1882-4)
    Marketing Start Date 2022-02-14
    NDC Exclude Flag N
    Pricing Information N/A