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    NDC 70518-1514-01 ATORVASTATIN CALCIUM 80 mg/1 Details

    ATORVASTATIN CALCIUM 80 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 PROPYLENE GLYCOL SOLVATE.

    Product Information

    NDC 70518-1514
    Product ID 70518-1514_02e6f01d-5153-aad7-e063-6294a90a0946
    Associated GPIs 39400010100350
    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 80
    Active Ingredient Units mg/1
    Substance Name ATORVASTATIN CALCIUM PROPYLENE GLYCOL SOLVATE
    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 ANDA090548
    Listing Certified Through 2024-12-31

    Package

    NDC 70518-1514-01 (70518151401)

    NDC Package Code 70518-1514-1
    Billing NDC 70518151401
    Package 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-1514-1)
    Marketing Start Date 2018-10-19
    NDC Exclude Flag N
    Pricing Information N/A