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    NDC 70518-3339-00 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 REMEDYREPACK INC.. The primary component is ATORVASTATIN CALCIUM TRIHYDRATE.

    Product Information

    NDC 70518-3339
    Product ID 70518-3339_0cf2a167-9fbc-f1e4-e063-6394a90a653d
    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 REMEDYREPACK INC.
    Pharmaceutical Class HMG-CoA Reductase Inhibitor [EPC], Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA211933
    Listing Certified Through 2024-12-31

    Package

    NDC 70518-3339-00 (70518333900)

    NDC Package Code 70518-3339-0
    Billing NDC 70518333900
    Package 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-3339-0)
    Marketing Start Date 2022-01-23
    NDC Exclude Flag N
    Pricing Information N/A