Search by Drug Name or NDC

    NDC 71335-0268-05 Hydroxyzine hydrochloride 10 mg/1 Details

    Hydroxyzine hydrochloride 10 mg/1

    Hydroxyzine hydrochloride is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Bryant Ranch Prepack. The primary component is HYDROXYZINE DIHYDROCHLORIDE.

    Product Information

    NDC 71335-0268
    Product ID 71335-0268_f24f2f99-f6fb-4ead-91ac-bfefcc93c2ed
    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
    Route ORAL
    Active Ingredient Strength 10
    Active Ingredient Units mg/1
    Substance Name HYDROXYZINE DIHYDROCHLORIDE
    Labeler Name Bryant Ranch Prepack
    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 71335-0268-05 (71335026805)

    NDC Package Code 71335-0268-5
    Billing NDC 71335026805
    Package 15 TABLET in 1 BOTTLE (71335-0268-5)
    Marketing Start Date 2022-02-02
    NDC Exclude Flag N
    Pricing Information N/A