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    NDC 68788-7056-06 Lovastatin 10 mg/1 Details

    Lovastatin 10 mg/1

    Lovastatin is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Preferred Pharmaceuticals Inc.. The primary component is LOVASTATIN.

    Product Information

    NDC 68788-7056
    Product ID 68788-7056_4f8a14bc-3825-4c94-bf93-7f94fa6ffe7a
    Associated GPIs 39400050000305
    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 Lovastatin
    Proprietary Name Suffix n/a
    Non-Proprietary Name Lovastatin
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET
    Route ORAL
    Active Ingredient Strength 10
    Active Ingredient Units mg/1
    Substance Name LOVASTATIN
    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 ANDA075991
    Listing Certified Through 2024-12-31

    Package

    NDC 68788-7056-06 (68788705606)

    NDC Package Code 68788-7056-6
    Billing NDC 68788705606
    Package 60 TABLET in 1 BOTTLE (68788-7056-6)
    Marketing Start Date 2018-01-05
    NDC Exclude Flag N
    Pricing Information N/A