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    NDC 49035-0739-27 Lansoprazole 15 mg/1 Details

    Lansoprazole 15 mg/1

    Lansoprazole is a ORAL CAPSULE, DELAYED RELEASE in the HUMAN OTC DRUG category. It is labeled and distributed by Wal-Mart Stores Inc. The primary component is LANSOPRAZOLE.

    Product Information

    NDC 49035-0739
    Product ID 49035-739_3a306bc1-5faa-c59d-6725-652b1ed8638a
    Associated GPIs 49270040006510
    GCN Sequence Number 030106
    GCN Sequence Number Description lansoprazole CAPSULE DR 15 MG ORAL
    HIC3 D4J
    HIC3 Description PROTON-PUMP INHIBITORS
    GCN 01697
    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 OTC DRUG
    Dosage Form CAPSULE, DELAYED RELEASE
    Route ORAL
    Active Ingredient Strength 15
    Active Ingredient Units mg/1
    Substance Name LANSOPRAZOLE
    Labeler Name Wal-Mart Stores Inc
    Pharmaceutical Class Inhibition Gastric Acid Secretion [PE], Proton Pump Inhibitor [EPC], Proton Pump Inhibitors [MoA]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA202194
    Listing Certified Through 2024-12-31

    Package

    NDC 49035-0739-27 (49035073927)

    NDC Package Code 49035-739-27
    Billing NDC 49035073927
    Package 2 BOTTLE in 1 PACKAGE, COMBINATION (49035-739-27) / 14 CAPSULE, DELAYED RELEASE in 1 BOTTLE (49035-739-52)
    Marketing Start Date 2012-05-18
    NDC Exclude Flag N
    Pricing Information N/A