Search by Drug Name or NDC

    NDC 63629-3583-03 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 Bryant Ranch Prepack. The primary component is LOVASTATIN.

    Product Information

    NDC 63629-3583
    Product ID 63629-3583_7fd9d5c7-8025-4049-8b5b-ae3d22db507f
    Associated GPIs 39400050000305
    GCN Sequence Number 016310
    GCN Sequence Number Description lovastatin TABLET 10 MG ORAL
    HIC3 M4D
    HIC3 Description ANTIHYPERLIPIDEMIC-HMGCOA REDUCTASE INHIB(STATINS)
    GCN 47042
    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 10
    Active Ingredient Units mg/1
    Substance Name LOVASTATIN
    Labeler Name Bryant Ranch Prepack
    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 2023-12-31

    Package

    NDC 63629-3583-03 (63629358303)

    NDC Package Code 63629-3583-3
    Billing NDC 63629358303
    Package 90 TABLET in 1 BOTTLE (63629-3583-3)
    Marketing Start Date 2011-08-09
    NDC Exclude Flag N
    Pricing Information N/A

    Standard Product Labeling (SPL)/Prescribing Information SPL 7fd9d5c7-8025-4049-8b5b-ae3d22db507f Details

    Revised: 1/2022