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    NDC 64380-0182-02 Omeprazole/Sodium Bicarbonate 20; 1680 mg/1700mg; mg/1700mg Details

    Omeprazole/Sodium Bicarbonate 20; 1680 mg/1700mg; mg/1700mg

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

    Product Information

    NDC 64380-0182
    Product ID 64380-182_2ac68a93-2f3b-46aa-a874-c109ad1bfefe
    Associated GPIs
    GCN Sequence Number 060473
    GCN Sequence Number Description omeprazole/sodium bicarbonate PACKET 20-1680MG ORAL
    HIC3 D4J
    HIC3 Description PROTON-PUMP INHIBITORS
    GCN 26634
    HICL Sequence Number 033512
    HICL Sequence Number Description OMEPRAZOLE/SODIUM BICARBONATE
    Brand/Generic Generic
    Proprietary Name Omeprazole/Sodium Bicarbonate
    Proprietary Name Suffix n/a
    Non-Proprietary Name omeprazole
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form POWDER, FOR SUSPENSION
    Route ORAL
    Active Ingredient Strength 20; 1680
    Active Ingredient Units mg/1700mg; mg/1700mg
    Substance Name OMEPRAZOLE; SODIUM BICARBONATE
    Labeler Name Strides Pharma Science Limited
    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 ANDA079182
    Listing Certified Through 2024-12-31

    Package

    NDC 64380-0182-02 (64380018202)

    NDC Package Code 64380-182-02
    Billing NDC 64380018202
    Package 30 POUCH in 1 CARTON (64380-182-02) / 20 mg in 1 POUCH (64380-182-01)
    Marketing Start Date 2022-10-01
    NDC Exclude Flag N
    Pricing Information N/A