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    NDC 71205-0984-60 Omeprazole/Bicarbonate 20; 1100 mg/1; mg/1 Details

    Omeprazole/Bicarbonate 20; 1100 mg/1; mg/1

    Omeprazole/Bicarbonate is a ORAL CAPSULE, GELATIN COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Proficient Rx LP. The primary component is OMEPRAZOLE; SODIUM BICARBONATE.

    Product Information

    NDC 71205-0984
    Product ID 71205-984_f35ea0c8-7b13-4fe6-9b43-2bbcb916250d
    Associated GPIs 49996002600120
    GCN Sequence Number 060471
    GCN Sequence Number Description omeprazole/sodium bicarbonate CAPSULE 20MG-1.1G ORAL
    HIC3 D4J
    HIC3 Description PROTON-PUMP INHIBITORS
    GCN 26632
    HICL Sequence Number 033512
    HICL Sequence Number Description OMEPRAZOLE/SODIUM BICARBONATE
    Brand/Generic Generic
    Proprietary Name Omeprazole/Bicarbonate
    Proprietary Name Suffix n/a
    Non-Proprietary Name Omeprazole and Sodium Bicarbonate
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form CAPSULE, GELATIN COATED
    Route ORAL
    Active Ingredient Strength 20; 1100
    Active Ingredient Units mg/1; mg/1
    Substance Name OMEPRAZOLE; SODIUM BICARBONATE
    Labeler Name Proficient Rx LP
    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 71205-0984-60 (71205098460)

    NDC Package Code 71205-984-60
    Billing NDC 71205098460
    Package 60 CAPSULE, GELATIN COATED in 1 BOTTLE, PLASTIC (71205-984-60)
    Marketing Start Date 2020-05-01
    NDC Exclude Flag N
    Pricing Information N/A