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    NDC 71205-0613-06 Omeprazole 20 mg/1 Details

    Omeprazole 20 mg/1

    Omeprazole is a ORAL CAPSULE, DELAYED RELEASE in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Proficient Rx LP. The primary component is OMEPRAZOLE.

    Product Information

    NDC 71205-0613
    Product ID 71205-613_d870bdc1-5e26-4153-89e2-f629fef60ad0
    Associated GPIs 49270060006520
    GCN Sequence Number 033530
    GCN Sequence Number Description omeprazole CAPSULE DR 20 MG ORAL
    HIC3 D4J
    HIC3 Description PROTON-PUMP INHIBITORS
    GCN 04348
    HICL Sequence Number 004673
    HICL Sequence Number Description OMEPRAZOLE
    Brand/Generic Generic
    Proprietary Name Omeprazole
    Proprietary Name Suffix n/a
    Non-Proprietary Name Omeprazole
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form CAPSULE, DELAYED RELEASE
    Route ORAL
    Active Ingredient Strength 20
    Active Ingredient Units mg/1
    Substance Name OMEPRAZOLE
    Labeler Name Proficient Rx LP
    Pharmaceutical Class Cytochrome P450 2C19 Inhibitors [MoA], Proton Pump Inhibitor [EPC], Proton Pump Inhibitors [MoA]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA212977
    Listing Certified Through 2024-12-31

    Package

    NDC 71205-0613-06 (71205061306)

    NDC Package Code 71205-613-06
    Billing NDC 71205061306
    Package 6 CAPSULE, DELAYED RELEASE in 1 BOTTLE (71205-613-06)
    Marketing Start Date 2023-08-14
    NDC Exclude Flag N
    Pricing Information N/A