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    NDC 50228-0364-05 Omeprazole and Sodium Bicarbonate 40; 1100 mg/1; mg/1 Details

    Omeprazole and Sodium Bicarbonate 40; 1100 mg/1; mg/1

    Omeprazole and Sodium Bicarbonate is a ORAL CAPSULE in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by ScieGen Pharmaceuticals, Inc.. The primary component is OMEPRAZOLE; SODIUM BICARBONATE.

    Product Information

    NDC 50228-0364
    Product ID 50228-364_0980fd8e-c1e1-5473-e063-6294a90aaf5e
    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 Omeprazole and Sodium Bicarbonate
    Proprietary Name Suffix n/a
    Non-Proprietary Name Omeprazole and Sodium Bicarbonate
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form CAPSULE
    Route ORAL
    Active Ingredient Strength 40; 1100
    Active Ingredient Units mg/1; mg/1
    Substance Name OMEPRAZOLE; SODIUM BICARBONATE
    Labeler Name ScieGen Pharmaceuticals, 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 ANDA
    Application Number ANDA207476
    Listing Certified Through 2024-12-31

    Package

    NDC 50228-0364-05 (50228036405)

    NDC Package Code 50228-364-05
    Billing NDC 50228036405
    Package 500 CAPSULE in 1 BOTTLE (50228-364-05)
    Marketing Start Date 2016-12-06
    NDC Exclude Flag N
    Pricing Information N/A