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    NDC 68682-0991-30 Omeprazole and Sodium Bicarbonate 40; 1680 mg/1; mg/1 Details

    Omeprazole and Sodium Bicarbonate 40; 1680 mg/1; mg/1

    Omeprazole and Sodium Bicarbonate is a ORAL POWDER, FOR SUSPENSION in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Oceanside Pharmaceuticals. The primary component is OMEPRAZOLE; SODIUM BICARBONATE.

    Product Information

    NDC 68682-0991
    Product ID 68682-991_0772e77f-5a7a-e170-e063-6394a90a1272
    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 Generic
    Proprietary Name Omeprazole and Sodium Bicarbonate
    Proprietary Name Suffix n/a
    Non-Proprietary Name omeprazole, 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 Oceanside Pharmaceuticals
    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 AUTHORIZED GENERIC
    Application Number NDA021636
    Listing Certified Through 2024-12-31

    Package

    NDC 68682-0991-30 (68682099130)

    NDC Package Code 68682-991-30
    Billing NDC 68682099130
    Package 30 PACKET in 1 CARTON (68682-991-30) / 1 POWDER, FOR SUSPENSION in 1 PACKET
    Marketing Start Date 2004-06-15
    NDC Exclude Flag N
    Pricing Information N/A