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    NDC 51655-0387-52 SIMVASTATIN 40 mg/1 Details

    SIMVASTATIN 40 mg/1

    SIMVASTATIN is a ORAL TABLET, FILM COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Northwind Pharmaceuticals, LLC. The primary component is SIMVASTATIN.

    Product Information

    NDC 51655-0387
    Product ID 51655-387_f8353a61-951c-6af7-e053-6294a90afdaa
    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 SIMVASTATIN
    Proprietary Name Suffix n/a
    Non-Proprietary Name SIMVASTATIN
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET, FILM COATED
    Route ORAL
    Active Ingredient Strength 40
    Active Ingredient Units mg/1
    Substance Name SIMVASTATIN
    Labeler Name Northwind Pharmaceuticals, LLC
    Pharmaceutical Class HMG-CoA Reductase Inhibitor [EPC], Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA078103
    Listing Certified Through 2024-12-31

    Package

    NDC 51655-0387-52 (51655038752)

    NDC Package Code 51655-387-52
    Billing NDC 51655038752
    Package 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-387-52)
    Marketing Start Date 2023-03-28
    NDC Exclude Flag N
    Pricing Information N/A