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    NDC 60760-0585-30 SIMVASTATIN 20 mg/1 Details

    SIMVASTATIN 20 mg/1

    SIMVASTATIN is a ORAL TABLET, FILM COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by ST. MARY'S MEDICAL PARK PHARMACY. The primary component is SIMVASTATIN.

    Product Information

    NDC 60760-0585
    Product ID 60760-585_faa81dcb-64df-3f43-e053-6394a90a485b
    Associated GPIs
    GCN Sequence Number 016578
    GCN Sequence Number Description simvastatin TABLET 20 MG ORAL
    HIC3 M4D
    HIC3 Description ANTIHYPERLIPIDEMIC-HMGCOA REDUCTASE INHIB(STATINS)
    GCN 26533
    HICL Sequence Number 006312
    HICL Sequence Number Description SIMVASTATIN
    Brand/Generic Generic
    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 20
    Active Ingredient Units mg/1
    Substance Name SIMVASTATIN
    Labeler Name ST. MARY'S MEDICAL PARK PHARMACY
    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 60760-0585-30 (60760058530)

    NDC Package Code 60760-585-30
    Billing NDC 60760058530
    Package 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-585-30)
    Marketing Start Date 2023-04-20
    NDC Exclude Flag N
    Pricing Information N/A