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    NDC 72189-0302-30 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 DirectRx. The primary component is MECLIZINE HYDROCHLORIDE.

    Product Information

    NDC 72189-0302
    Product ID 72189-302_db709a98-70ca-11a2-e053-2995a90af78d
    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 DirectRx
    Pharmaceutical Class Antiemetic [EPC], Emesis Suppression [PE]
    DEA Schedule n/a
    Marketing Category NDA AUTHORIZED GENERIC
    Application Number NDA010721
    Listing Certified Through 2024-12-31

    Package

    NDC 72189-0302-30 (72189030230)

    NDC Package Code 72189-302-30
    Billing NDC 72189030230
    Package 30 TABLET in 1 BOTTLE (72189-302-30)
    Marketing Start Date 2021-12-06
    NDC Exclude Flag N
    Pricing Information N/A

    Standard Product Labeling (SPL)/Prescribing Information SPL d27fe828-4fee-3ba9-e053-2995a90ae7b6 Details

    Revised: 3/2022