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    NDC 42708-0004-30 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 QPharma Inc. The primary component is ATORVASTATIN CALCIUM TRIHYDRATE.

    Product Information

    NDC 42708-0004
    Product ID 42708-004_026f9d94-f6dd-6e03-e063-6294a90a96b2
    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 QPharma Inc
    Pharmaceutical Class HMG-CoA Reductase Inhibitor [EPC], Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA205300
    Listing Certified Through 2024-12-31

    Package

    NDC 42708-0004-30 (42708000430)

    NDC Package Code 42708-004-30
    Billing NDC 42708000430
    Package 30 TABLET, FILM COATED in 1 BOTTLE (42708-004-30)
    Marketing Start Date 2018-05-31
    NDC Exclude Flag N
    Pricing Information N/A