Search by Drug Name or NDC

    NDC 42291-0475-60 Lubiprostone 8 ug/1 Details

    Lubiprostone 8 ug/1

    Lubiprostone is a ORAL CAPSULE in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by AvKARE. The primary component is LUBIPROSTONE.

    Product Information

    NDC 42291-0475
    Product ID 42291-475_f7a613ca-8beb-ef3f-e053-6294a90a14e7
    Associated GPIs
    GCN Sequence Number 063946
    GCN Sequence Number Description lubiprostone CAPSULE 8 MCG ORAL
    HIC3 D6S
    HIC3 Description LAXATIVES AND CATHARTICS
    GCN 99658
    HICL Sequence Number 033451
    HICL Sequence Number Description LUBIPROSTONE
    Brand/Generic Generic
    Proprietary Name Lubiprostone
    Proprietary Name Suffix n/a
    Non-Proprietary Name Lubiprostone
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form CAPSULE
    Route ORAL
    Active Ingredient Strength 8
    Active Ingredient Units ug/1
    Substance Name LUBIPROSTONE
    Labeler Name AvKARE
    Pharmaceutical Class Chloride Channel Activator [EPC], Chloride Channel Activators [MoA]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA209450
    Listing Certified Through 2024-12-31

    Package

    NDC 42291-0475-60 (42291047560)

    NDC Package Code 42291-475-60
    Billing NDC 42291047560
    Package 60 CAPSULE in 1 BOTTLE (42291-475-60)
    Marketing Start Date 2023-01-04
    NDC Exclude Flag N
    Pricing Information N/A