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    NDC 68012-0054-30 ZEGERID 40; 1680 mg/1; mg/1 Details

    ZEGERID 40; 1680 mg/1; mg/1

    ZEGERID is a ORAL POWDER, FOR SUSPENSION in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Santarus, Inc... The primary component is OMEPRAZOLE; SODIUM BICARBONATE.

    Product Information

    NDC 68012-0054
    Product ID 68012-054_bc93408c-bea8-429d-a2f9-d587fd3204c3
    Associated GPIs 49996002603040
    GCN Sequence Number 060474
    GCN Sequence Number Description omeprazole/sodium bicarbonate PACKET 40-1680MG ORAL
    HIC3 D4J
    HIC3 Description PROTON-PUMP INHIBITORS
    GCN 26635
    HICL Sequence Number 033512
    HICL Sequence Number Description OMEPRAZOLE/SODIUM BICARBONATE
    Brand/Generic Brand
    Proprietary Name ZEGERID
    Proprietary Name Suffix n/a
    Non-Proprietary Name omeprazole and sodium bicarbonate
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form POWDER, FOR SUSPENSION
    Route ORAL
    Active Ingredient Strength 40; 1680
    Active Ingredient Units mg/1; mg/1
    Substance Name OMEPRAZOLE; SODIUM BICARBONATE
    Labeler Name Santarus, Inc..
    Pharmaceutical Class Alkalinizing Activity [MoA], Cytochrome P450 2C19 Inhibitors [MoA], Proton Pump Inhibitor [EPC], Proton Pump Inhibitors [MoA]
    DEA Schedule n/a
    Marketing Category NDA
    Application Number NDA021636
    Listing Certified Through 2024-12-31

    Package

    NDC 68012-0054-30 (68012005430)

    NDC Package Code 68012-054-30
    Billing NDC 68012005430
    Package 30 PACKET in 1 CARTON (68012-054-30) / 1 POWDER, FOR SUSPENSION in 1 PACKET
    Marketing Start Date 2014-06-15
    NDC Exclude Flag N
    Pricing Information N/A