Search by Drug Name or NDC

    NDC 69680-0161-30 Memantine Hydrochloride 7 mg/1 Details

    Memantine Hydrochloride 7 mg/1

    Memantine Hydrochloride is a ORAL CAPSULE, EXTENDED RELEASE in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Vitruvias Therapeutics. The primary component is MEMANTINE HYDROCHLORIDE.

    Product Information

    NDC 69680-0161
    Product ID 69680-161_6d571abb-865b-4a76-874f-c9ba6369267b
    Associated GPIs
    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 Memantine Hydrochloride
    Proprietary Name Suffix n/a
    Non-Proprietary Name memantine hydrochloride
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form CAPSULE, EXTENDED RELEASE
    Route ORAL
    Active Ingredient Strength 7
    Active Ingredient Units mg/1
    Substance Name MEMANTINE HYDROCHLORIDE
    Labeler Name Vitruvias Therapeutics
    Pharmaceutical Class N-methyl-D-aspartate Receptor Antagonist [EPC], NMDA Receptor Antagonists [MoA]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA213985
    Listing Certified Through 2024-12-31

    Package

    NDC 69680-0161-30 (69680016130)

    NDC Package Code 69680-161-30
    Billing NDC 69680016130
    Package 30 CAPSULE, EXTENDED RELEASE in 1 BOTTLE (69680-161-30)
    Marketing Start Date 2023-12-15
    NDC Exclude Flag N
    Pricing Information N/A