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    NDC 63629-2432-01 MECLIZINE HYDROCHLORIDE 12.5 mg/1 Details

    MECLIZINE HYDROCHLORIDE 12.5 mg/1

    MECLIZINE HYDROCHLORIDE is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Bryant Ranch Prepack. The primary component is MECLIZINE HYDROCHLORIDE.

    Product Information

    NDC 63629-2432
    Product ID 63629-2432_09070485-0913-47b5-8204-c960757d34df
    Associated GPIs 50200050000305
    GCN Sequence Number 004731
    GCN Sequence Number Description meclizine HCl TABLET 12.5 MG ORAL
    HIC3 H6J
    HIC3 Description ANTIEMETIC/ANTIVERTIGO AGENTS
    GCN 18301
    HICL Sequence Number 001975
    HICL Sequence Number Description MECLIZINE HCL
    Brand/Generic Generic
    Proprietary Name MECLIZINE HYDROCHLORIDE
    Proprietary Name Suffix n/a
    Non-Proprietary Name Meclizine Hydrochloride
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET
    Route ORAL
    Active Ingredient Strength 12.5
    Active Ingredient Units mg/1
    Substance Name MECLIZINE HYDROCHLORIDE
    Labeler Name Bryant Ranch Prepack
    Pharmaceutical Class Antiemetic [EPC], Emesis Suppression [PE]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA040659
    Listing Certified Through 2024-12-31

    Package

    NDC 63629-2432-01 (63629243201)

    NDC Package Code 63629-2432-1
    Billing NDC 63629243201
    Package 1000 TABLET in 1 BOTTLE (63629-2432-1)
    Marketing Start Date 2021-02-25
    NDC Exclude Flag N
    Pricing Information N/A