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    NDC 71205-0603-90 RABEPRAZOLE SODIUM 20 mg/1 Details

    RABEPRAZOLE SODIUM 20 mg/1

    RABEPRAZOLE SODIUM is a ORAL TABLET, DELAYED RELEASE in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Proficient Rx LP. The primary component is RABEPRAZOLE SODIUM.

    Product Information

    NDC 71205-0603
    Product ID 71205-603_ddba7982-5cbb-4a0f-9425-542cb118e9fa
    Associated GPIs 49270076100620
    GCN Sequence Number 040941
    GCN Sequence Number Description rabeprazole sodium TABLET DR 20 MG ORAL
    HIC3 D4J
    HIC3 Description PROTON-PUMP INHIBITORS
    GCN 94639
    HICL Sequence Number 018847
    HICL Sequence Number Description RABEPRAZOLE SODIUM
    Brand/Generic Generic
    Proprietary Name RABEPRAZOLE SODIUM
    Proprietary Name Suffix n/a
    Non-Proprietary Name rabeprazole sodium
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET, DELAYED RELEASE
    Route ORAL
    Active Ingredient Strength 20
    Active Ingredient Units mg/1
    Substance Name RABEPRAZOLE SODIUM
    Labeler Name Proficient Rx LP
    Pharmaceutical Class Proton Pump Inhibitor [EPC], Proton Pump Inhibitors [MoA]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA204237
    Listing Certified Through 2024-12-31

    Package

    NDC 71205-0603-90 (71205060390)

    NDC Package Code 71205-603-90
    Billing NDC 71205060390
    Package 90 TABLET, DELAYED RELEASE in 1 BOTTLE (71205-603-90)
    Marketing Start Date 2021-09-14
    NDC Exclude Flag N
    Pricing Information N/A

    Standard Product Labeling (SPL)/Prescribing Information SPL 0f5eb1b4-ad4b-4782-8d3d-cd33f9c5be7d Details

    Revised: 4/2022