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    NDC 53002-1335-09 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 RPK Pharmaceuticals, Inc.. The primary component is ATORVASTATIN CALCIUM TRIHYDRATE.

    Product Information

    NDC 53002-1335
    Product ID 53002-1335_44f92004-25d6-4758-a16d-e2b1060c44d4
    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 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 TRIHYDRATE
    Labeler Name RPK Pharmaceuticals, Inc.
    Pharmaceutical Class HMG-CoA Reductase Inhibitor [EPC], Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA091624
    Listing Certified Through 2024-12-31

    Package

    NDC 53002-1335-09 (53002133509)

    NDC Package Code 53002-1335-9
    Billing NDC 53002133509
    Package 90 TABLET, FILM COATED in 1 BOTTLE (53002-1335-9)
    Marketing Start Date 2017-09-01
    NDC Exclude Flag N
    Pricing Information N/A