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    NDC 63187-0996-10 MECLIZINE HYDROCHLORIDE 25 mg/1 Details

    MECLIZINE HYDROCHLORIDE 25 mg/1

    MECLIZINE HYDROCHLORIDE is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Proficient Rx LP. The primary component is MECLIZINE HYDROCHLORIDE.

    Product Information

    NDC 63187-0996
    Product ID 63187-996_6d44d894-810c-4608-a503-0cc6ff1f965d
    Associated GPIs 50200050000310
    GCN Sequence Number 004732
    GCN Sequence Number Description meclizine HCl TABLET 25 MG ORAL
    HIC3 H6J
    HIC3 Description ANTIEMETIC/ANTIVERTIGO AGENTS
    GCN 18302
    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 Hydrocloride
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET
    Route ORAL
    Active Ingredient Strength 25
    Active Ingredient Units mg/1
    Substance Name MECLIZINE HYDROCHLORIDE
    Labeler Name Proficient Rx LP
    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 63187-0996-10 (63187099610)

    NDC Package Code 63187-996-10
    Billing NDC 63187099610
    Package 10 TABLET in 1 BOTTLE (63187-996-10)
    Marketing Start Date 2020-05-12
    NDC Exclude Flag N
    Pricing Information N/A

    Standard Product Labeling (SPL)/Prescribing Information SPL f574e123-8db7-4e3d-a0ee-e4e1f04ff146 Details

    Revised: 6/2022