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    NDC 71335-1820-08 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 Bryant Ranch Prepack. The primary component is LANSOPRAZOLE.

    Product Information

    NDC 71335-1820
    Product ID 71335-1820_e66cf5f3-d909-40ad-a03d-c0423f41aa23
    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 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 Bryant Ranch Prepack
    Pharmaceutical Class Inhibition Gastric Acid Secretion [PE], Proton Pump Inhibitor [EPC], Proton Pump Inhibitors [MoA]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA203203
    Listing Certified Through 2024-12-31

    Package

    NDC 71335-1820-08 (71335182008)

    NDC Package Code 71335-1820-8
    Billing NDC 71335182008
    Package 180 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71335-1820-8)
    Marketing Start Date 2022-07-06
    NDC Exclude Flag N
    Pricing Information N/A