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    NDC 71335-1891-03 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 Bryant Ranch Prepack. The primary component is SIMVASTATIN.

    Product Information

    NDC 71335-1891
    Product ID 71335-1891_b410c937-f9a1-4089-8ede-265c2dbc32d4
    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 20
    Active Ingredient Units mg/1
    Substance Name SIMVASTATIN
    Labeler Name Bryant Ranch Prepack
    Pharmaceutical Class HMG-CoA Reductase Inhibitor [EPC], Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA078034
    Listing Certified Through 2024-12-31

    Package

    NDC 71335-1891-03 (71335189103)

    NDC Package Code 71335-1891-3
    Billing NDC 71335189103
    Package 100 TABLET, FILM COATED in 1 BOTTLE (71335-1891-3)
    Marketing Start Date 2021-12-29
    NDC Exclude Flag N
    Pricing Information N/A