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    NDC 43063-0627-28 Hydroxyzine Hydrochloride 25 mg/1 Details

    Hydroxyzine Hydrochloride 25 mg/1

    Hydroxyzine Hydrochloride is a ORAL TABLET, FILM COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by PD-Rx Pharmaceuticals, Inc.. The primary component is HYDROXYZINE DIHYDROCHLORIDE.

    Product Information

    NDC 43063-0627
    Product ID 43063-627_f67f6c63-ae04-0d27-e053-2a95a90a9c10
    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 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 25
    Active Ingredient Units mg/1
    Substance Name HYDROXYZINE DIHYDROCHLORIDE
    Labeler Name PD-Rx Pharmaceuticals, Inc.
    Pharmaceutical Class Antihistamine [EPC], Histamine Receptor Antagonists [MoA]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA040786
    Listing Certified Through 2024-12-31

    Package

    NDC 43063-0627-28 (43063062728)

    NDC Package Code 43063-627-28
    Billing NDC 43063062728
    Package 28 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-627-28)
    Marketing Start Date 2015-10-28
    NDC Exclude Flag N
    Pricing Information N/A