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    NDC 67877-0275-30 Lansoprazole 30 mg/1 Details

    Lansoprazole 30 mg/1

    Lansoprazole is a ORAL CAPSULE, DELAYED RELEASE in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Ascend Laboratories, LLC. The primary component is LANSOPRAZOLE.

    Product Information

    NDC 67877-0275
    Product ID 67877-275_9d59dfb2-038e-480f-8d9a-84141952f81b
    Associated GPIs 49270040006520
    GCN Sequence Number 030107
    GCN Sequence Number Description lansoprazole CAPSULE DR 30 MG ORAL
    HIC3 D4J
    HIC3 Description PROTON-PUMP INHIBITORS
    GCN 01698
    HICL Sequence Number 008993
    HICL Sequence Number Description LANSOPRAZOLE
    Brand/Generic Generic
    Proprietary Name Lansoprazole
    Proprietary Name Suffix n/a
    Non-Proprietary Name Lansoprazole
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form CAPSULE, DELAYED RELEASE
    Route ORAL
    Active Ingredient Strength 30
    Active Ingredient Units mg/1
    Substance Name LANSOPRAZOLE
    Labeler Name Ascend Laboratories, LLC
    Pharmaceutical Class Inhibition Gastric Acid Secretion [PE], Proton Pump Inhibitor [EPC], Proton Pump Inhibitors [MoA]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA207394
    Listing Certified Through 2024-12-31

    Package

    NDC 67877-0275-30 (67877027530)

    NDC Package Code 67877-275-30
    Billing NDC 67877027530
    Package 30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (67877-275-30)
    Marketing Start Date 2019-01-20
    NDC Exclude Flag N
    Pricing Information N/A