Search by Drug Name or NDC

    NDC 71205-0994-00 Lovastatin 40 mg/1 Details

    Lovastatin 40 mg/1

    Lovastatin is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Proficient Rx LP. The primary component is LOVASTATIN.

    Product Information

    NDC 71205-0994
    Product ID 71205-994_e637904d-8af6-47fe-b10e-db813d5531bc
    Associated GPIs 39400050000320
    GCN Sequence Number 006461
    GCN Sequence Number Description lovastatin TABLET 40 MG ORAL
    HIC3 M4D
    HIC3 Description ANTIHYPERLIPIDEMIC-HMGCOA REDUCTASE INHIB(STATINS)
    GCN 47041
    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 40
    Active Ingredient Units mg/1
    Substance Name LOVASTATIN
    Labeler Name Proficient Rx LP
    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 71205-0994-00 (71205099400)

    NDC Package Code 71205-994-00
    Billing NDC 71205099400
    Package 100 TABLET in 1 BOTTLE (71205-994-00)
    Marketing Start Date 2020-04-01
    NDC Exclude Flag N
    Pricing Information N/A

    Standard Product Labeling (SPL)/Prescribing Information SPL 25efd38a-1495-4824-9137-a3429bc471bd Details

    Revised: 7/2022