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    NDC 55154-4232-00 Protonix 40 mg/1 Details

    Protonix 40 mg/1

    Protonix is a ORAL GRANULE, DELAYED RELEASE in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Cardinal Health 107, LLC. The primary component is PANTOPRAZOLE SODIUM.

    Product Information

    NDC 55154-4232
    Product ID 55154-4232_2fd2b436-0be8-4f80-8554-2f663bc8af80
    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 Protonix
    Proprietary Name Suffix Delayed-Release
    Non-Proprietary Name pantoprazole sodium
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form GRANULE, DELAYED RELEASE
    Route ORAL
    Active Ingredient Strength 40
    Active Ingredient Units mg/1
    Substance Name PANTOPRAZOLE SODIUM
    Labeler Name Cardinal Health 107, LLC
    Pharmaceutical Class Proton Pump Inhibitor [EPC], Proton Pump Inhibitors [MoA]
    DEA Schedule n/a
    Marketing Category NDA
    Application Number NDA022020
    Listing Certified Through 2024-12-31

    Package

    NDC 55154-4232-00 (55154423200)

    NDC Package Code 55154-4232-0
    Billing NDC 55154423200
    Package 10 PACKET in 1 BAG (55154-4232-0) / 40 GRANULE, DELAYED RELEASE in 1 PACKET
    Marketing Start Date 2008-02-29
    NDC Exclude Flag N
    Pricing Information N/A