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    NDC 68788-7742-01 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 Preferred Pharmaceuticals, Inc.. The primary component is LANSOPRAZOLE.

    Product Information

    NDC 68788-7742
    Product ID 68788-7742_7191d247-c504-47a3-827b-d724486d0dd7
    Associated GPIs 49270040006520
    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 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 Preferred Pharmaceuticals, 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 ANDA205868
    Listing Certified Through 2024-12-31

    Package

    NDC 68788-7742-01 (68788774201)

    NDC Package Code 68788-7742-1
    Billing NDC 68788774201
    Package 14 CAPSULE, DELAYED RELEASE in 1 BOTTLE (68788-7742-1)
    Marketing Start Date 2020-07-01
    NDC Exclude Flag N
    Pricing Information N/A