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    NDC 68788-7676-03 Hydroxyzine Hydrochloride 10 mg/1 Details

    Hydroxyzine Hydrochloride 10 mg/1

    Hydroxyzine Hydrochloride 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 HYDROXYZINE DIHYDROCHLORIDE.

    Product Information

    NDC 68788-7676
    Product ID 68788-7676_34f51202-01f6-487d-a6cf-daec0125f88c
    Associated GPIs 57200040100305
    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 Hydroxyzine Hydrochloride
    Proprietary Name Suffix n/a
    Non-Proprietary Name Hydroxyzine Hydrochloride
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET, FILM COATED
    Route ORAL
    Active Ingredient Strength 10
    Active Ingredient Units mg/1
    Substance Name HYDROXYZINE DIHYDROCHLORIDE
    Labeler Name Preferred Pharmaceuticals, Inc.
    Pharmaceutical Class Antihistamine [EPC], Histamine Receptor Antagonists [MoA]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA088617
    Listing Certified Through 2024-12-31

    Package

    NDC 68788-7676-03 (68788767603)

    NDC Package Code 68788-7676-3
    Billing NDC 68788767603
    Package 30 TABLET, FILM COATED in 1 BOTTLE (68788-7676-3)
    Marketing Start Date 2020-03-02
    NDC Exclude Flag N
    Pricing Information N/A
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