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    NDC 68788-7874-09 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 Preferred Pharmaceuticals Inc. The primary component is ATORVASTATIN CALCIUM PROPYLENE GLYCOL SOLVATE.

    Product Information

    NDC 68788-7874
    Product ID 68788-7874_52f97ead-1668-46e0-b3f2-987738c81f83
    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 PROPYLENE GLYCOL SOLVATE
    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 ANDA090548
    Listing Certified Through 2024-12-31

    Package

    NDC 68788-7874-09 (68788787409)

    NDC Package Code 68788-7874-9
    Billing NDC 68788787409
    Package 90 TABLET, FILM COATED in 1 BOTTLE (68788-7874-9)
    Marketing Start Date 2021-03-08
    NDC Exclude Flag N
    Pricing Information N/A