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    NDC 43598-0883-52 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 Dr. Reddy's Laboratories Inc.. The primary component is LANSOPRAZOLE.

    Product Information

    NDC 43598-0883
    Product ID 43598-883_4ccf5ed3-aaf3-0ff8-adab-0f395e7bb7eb
    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 OTC DRUG
    Dosage Form CAPSULE, DELAYED RELEASE
    Route ORAL
    Active Ingredient Strength 15
    Active Ingredient Units mg/1
    Substance Name LANSOPRAZOLE
    Labeler Name Dr. Reddy's Laboratories 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 43598-0883-52 (43598088352)

    NDC Package Code 43598-883-52
    Billing NDC 43598088352
    Package 1 BOTTLE in 1 CARTON (43598-883-52) / 14 CAPSULE, DELAYED RELEASE in 1 BOTTLE
    Marketing Start Date 2019-08-01
    NDC Exclude Flag N
    Pricing Information N/A