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    NDC 68788-7854-03 Hydroxyzine hydrochloride 25 mg/1 Details

    Hydroxyzine hydrochloride 25 mg/1

    Hydroxyzine hydrochloride is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Preferred Pharmaceuticals Incl. The primary component is HYDROXYZINE DIHYDROCHLORIDE.

    Product Information

    NDC 68788-7854
    Product ID 68788-7854_089b6097-a264-46f5-9395-1c321083bb29
    Associated GPIs 57200040100310
    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
    Route ORAL
    Active Ingredient Strength 25
    Active Ingredient Units mg/1
    Substance Name HYDROXYZINE DIHYDROCHLORIDE
    Labeler Name Preferred Pharmaceuticals Incl
    Pharmaceutical Class Antihistamine [EPC], Histamine Receptor Antagonists [MoA]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA204279
    Listing Certified Through 2024-12-31

    Package

    NDC 68788-7854-03 (68788785403)

    NDC Package Code 68788-7854-3
    Billing NDC 68788785403
    Package 30 TABLET in 1 BOTTLE (68788-7854-3)
    Marketing Start Date 2021-01-29
    NDC Exclude Flag N
    Pricing Information N/A