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    NDC 51655-0119-52 Hydroxyzine hydrochloride 50 mg/1 Details

    Hydroxyzine hydrochloride 50 mg/1

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

    Product Information

    NDC 51655-0119
    Product ID 51655-119_f2b3d15f-d73d-9dd1-e053-2a95a90a6bb0
    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
    Route ORAL
    Active Ingredient Strength 50
    Active Ingredient Units mg/1
    Substance Name HYDROXYZINE DIHYDROCHLORIDE
    Labeler Name Northwind Pharmaceuticals, LLC
    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 51655-0119-52 (51655011952)

    NDC Package Code 51655-119-52
    Billing NDC 51655011952
    Package 30 TABLET in 1 BOTTLE, PLASTIC (51655-119-52)
    Marketing Start Date 2022-08-16
    NDC Exclude Flag N
    Pricing Information N/A