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    NDC 16571-0698-01 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 Rising Pharma Holdings, Inc.. The primary component is LANSOPRAZOLE.

    Product Information

    NDC 16571-0698
    Product ID 16571-698_b62ff2cb-32d6-4056-badb-343f922b3a21
    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 Rising Pharma Holdings, 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 ANDA201921
    Listing Certified Through 2024-12-31

    Package

    NDC 16571-0698-01 (16571069801)

    NDC Package Code 16571-698-01
    Billing NDC 16571069801
    Package 100 CAPSULE, DELAYED RELEASE in 1 BOTTLE (16571-698-01)
    Marketing Start Date 2020-01-11
    NDC Exclude Flag N
    Pricing Information N/A