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    NDC 43063-0692-90 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 PD-Rx Pharmaceuticals, Inc.. The primary component is LOVASTATIN.

    Product Information

    NDC 43063-0692
    Product ID 43063-692_01cacf24-9020-802e-e063-6294a90ac0ea
    Associated GPIs 39400050000310
    GCN Sequence Number 006460
    GCN Sequence Number Description lovastatin TABLET 20 MG ORAL
    HIC3 M4D
    HIC3 Description ANTIHYPERLIPIDEMIC-HMGCOA REDUCTASE INHIB(STATINS)
    GCN 47040
    HICL Sequence Number 002793
    HICL Sequence Number Description LOVASTATIN
    Brand/Generic Generic
    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 PD-Rx 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 43063-0692-90 (43063069290)

    NDC Package Code 43063-692-90
    Billing NDC 43063069290
    Package 90 TABLET in 1 BOTTLE, PLASTIC (43063-692-90)
    Marketing Start Date 2016-07-26
    NDC Exclude Flag N
    Pricing Information N/A