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    NDC 68788-7410-01 Paroxetine 30 mg/1 Details

    Paroxetine 30 mg/1

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

    Product Information

    NDC 68788-7410
    Product ID 68788-7410_0a97d86e-7048-48b0-90ba-6f1079afb93a
    Associated GPIs 58160060000330
    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 30
    Active Ingredient Units mg/1
    Substance Name PAROXETINE HYDROCHLORIDE
    Labeler Name Preferred Pharmaceuticals Inc.
    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 68788-7410-01 (68788741001)

    NDC Package Code 68788-7410-1
    Billing NDC 68788741001
    Package 100 TABLET, FILM COATED in 1 BOTTLE (68788-7410-1)
    Marketing Start Date 2018-06-06
    NDC Exclude Flag N
    Pricing Information N/A