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    NDC 68788-7631-01 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 Preferred Pharmaceuticals Inc.. The primary component is ATORVASTATIN CALCIUM TRIHYDRATE.

    Product Information

    NDC 68788-7631
    Product ID 68788-7631_9306c3e0-a260-4d70-9d65-e821a561492d
    Associated GPIs 39400010100320
    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 Preferred Pharmaceuticals Inc.
    Pharmaceutical Class HMG-CoA Reductase Inhibitor [EPC], Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA207687
    Listing Certified Through 2024-12-31

    Package

    NDC 68788-7631-01 (68788763101)

    NDC Package Code 68788-7631-1
    Billing NDC 68788763101
    Package 100 TABLET, FILM COATED in 1 BOTTLE (68788-7631-1)
    Marketing Start Date 2020-03-05
    NDC Exclude Flag N
    Pricing Information N/A