Search by Drug Name or NDC

    NDC 63187-0765-30 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 Proficient Rx LP. The primary component is LOVASTATIN.

    Product Information

    NDC 63187-0765
    Product ID 63187-765_045f5277-63a9-43c3-ae26-126a3ad3c16e
    Associated GPIs
    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 20
    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 ANDA078296
    Listing Certified Through 2024-12-31

    Package

    NDC 63187-0765-30 (63187076530)

    NDC Package Code 63187-765-30
    Billing NDC 63187076530
    Package 30 TABLET in 1 BOTTLE (63187-765-30)
    Marketing Start Date 2016-11-01
    NDC Exclude Flag N
    Pricing Information N/A