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    NDC 70518-2635-00 atorvastatin calcium 20 mg/1 Details

    atorvastatin calcium 20 mg/1

    atorvastatin calcium is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by REMEDYREPACK INC.. The primary component is ATORVASTATIN CALCIUM TRIHYDRATE.

    Product Information

    NDC 70518-2635
    Product ID 70518-2635_0c78d401-5df6-4dad-e063-6394a90ab5d1
    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, film coated
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET
    Route ORAL
    Active Ingredient Strength 20
    Active Ingredient Units mg/1
    Substance Name ATORVASTATIN CALCIUM TRIHYDRATE
    Labeler Name REMEDYREPACK INC.
    Pharmaceutical Class HMG-CoA Reductase Inhibitor [EPC], Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA209912
    Listing Certified Through 2024-12-31

    Package

    NDC 70518-2635-00 (70518263500)

    NDC Package Code 70518-2635-0
    Billing NDC 70518263500
    Package 30 TABLET in 1 BLISTER PACK (70518-2635-0)
    Marketing Start Date 2020-03-18
    NDC Exclude Flag N
    Pricing Information N/A