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    NDC 68180-0468-09 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 Lupin Pharmaceuticals, Inc.. The primary component is LOVASTATIN.

    Product Information

    NDC 68180-0468
    Product ID 68180-468_2a7b570f-e6b0-4311-abd0-c13a87a0b164
    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 Lupin 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 68180-0468-09 (68180046809)

    NDC Package Code 68180-468-09
    Billing NDC 68180046809
    Package 90 TABLET in 1 BOTTLE (68180-468-09)
    Marketing Start Date 2007-11-01
    NDC Exclude Flag N
    Pricing Information N/A