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    NDC 53002-1385-00 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 RPK Pharmaceuticals, Inc.. The primary component is LOVASTATIN.

    Product Information

    NDC 53002-1385
    Product ID 53002-1385_684947b5-38c4-4e68-81f6-3de935f4d19b
    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 RPK Pharmaceuticals, Inc.
    Pharmaceutical Class HMG-CoA Reductase Inhibitor [EPC], Hydroxymethylglutaryl-CoA Reductase Inhibitors [MoA]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA078296
    Listing Certified Through 2024-12-31

    Package

    NDC 53002-1385-00 (53002138500)

    NDC Package Code 53002-1385-0
    Billing NDC 53002138500
    Package 100 TABLET in 1 BOTTLE (53002-1385-0)
    Marketing Start Date 2017-09-01
    NDC Exclude Flag N
    Pricing Information N/A