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    NDC 71335-1051-03 ATORVASTATIN CALCIUM 20 mg/1 Details

    ATORVASTATIN CALCIUM 20 mg/1

    ATORVASTATIN CALCIUM 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 ATORVASTATIN CALCIUM PROPYLENE GLYCOL SOLVATE.

    Product Information

    NDC 71335-1051
    Product ID 71335-1051_37d3659f-cf80-4a21-a646-3e0edcda04a7
    Associated GPIs 39400010100320
    GCN Sequence Number 029968
    GCN Sequence Number Description atorvastatin calcium TABLET 20 MG ORAL
    HIC3 M4D
    HIC3 Description ANTIHYPERLIPIDEMIC-HMGCOA REDUCTASE INHIB(STATINS)
    GCN 43721
    HICL Sequence Number 012404
    HICL Sequence Number Description ATORVASTATIN CALCIUM
    Brand/Generic Generic
    Proprietary Name ATORVASTATIN CALCIUM
    Proprietary Name Suffix n/a
    Non-Proprietary Name ATORVASTATIN CALCIUM
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET, FILM COATED
    Route ORAL
    Active Ingredient Strength 20
    Active Ingredient Units mg/1
    Substance Name ATORVASTATIN CALCIUM PROPYLENE GLYCOL SOLVATE
    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 ANDA090548
    Listing Certified Through 2024-12-31

    Package

    NDC 71335-1051-03 (71335105103)

    NDC Package Code 71335-1051-3
    Billing NDC 71335105103
    Package 90 TABLET, FILM COATED in 1 BOTTLE (71335-1051-3)
    Marketing Start Date 2019-02-06
    NDC Exclude Flag N
    Pricing Information N/A