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    NDC 53746-0169-30 Memantine hydrochloride 10 mg/1 Details

    Memantine hydrochloride 10 mg/1

    Memantine hydrochloride is a ORAL TABLET, FILM COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Amneal Pharmaceuticals of New York LLC. The primary component is MEMANTINE HYDROCHLORIDE.

    Product Information

    NDC 53746-0169
    Product ID 53746-169_cf08de43-a887-40f3-a074-57ecc8d3093a
    Associated GPIs 62053550100330
    GCN Sequence Number 032492
    GCN Sequence Number Description memantine HCl TABLET 10 MG ORAL
    HIC3 H1A
    HIC3 Description ALZHEIMER'S THERAPY, NMDA RECEPTOR ANTAGONISTS
    GCN 03253
    HICL Sequence Number 013778
    HICL Sequence Number Description MEMANTINE HCL
    Brand/Generic Generic
    Proprietary Name Memantine hydrochloride
    Proprietary Name Suffix n/a
    Non-Proprietary Name Memantine
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET, FILM COATED
    Route ORAL
    Active Ingredient Strength 10
    Active Ingredient Units mg/1
    Substance Name MEMANTINE HYDROCHLORIDE
    Labeler Name Amneal Pharmaceuticals of New York LLC
    Pharmaceutical Class N-methyl-D-aspartate Receptor Antagonist [EPC], NMDA Receptor Antagonists [MoA]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA090041
    Listing Certified Through 2024-12-31

    Package

    NDC 53746-0169-30 (53746016930)

    NDC Package Code 53746-169-30
    Billing NDC 53746016930
    Package 30 TABLET, FILM COATED in 1 BOTTLE (53746-169-30)
    Marketing Start Date 2015-04-30
    NDC Exclude Flag N
    Pricing Information N/A