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    NDC 70934-0415-30 Lovastatin 20 mg/1 Details

    Lovastatin 20 mg/1

    Lovastatin is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Denton Pharma, Inc. DBA Northwind Pharmaceuticals. The primary component is LOVASTATIN.

    Product Information

    NDC 70934-0415
    Product ID 70934-415_cb9482aa-ccda-36e9-e053-2995a90aca82
    Associated GPIs 39400050000310
    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 20
    Active Ingredient Units mg/1
    Substance Name LOVASTATIN
    Labeler Name Denton Pharma, Inc. DBA Northwind Pharmaceuticals
    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 n/a

    Package

    NDC 70934-0415-30 (70934041530)

    NDC Package Code 70934-415-30
    Billing NDC 70934041530
    Package 30 TABLET in 1 BOTTLE, PLASTIC (70934-415-30)
    Marketing Start Date 2019-07-26
    NDC Exclude Flag N
    Pricing Information N/A
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