Search by Drug Name or NDC

    NDC 71713-0301-01 omeprazole 20 mg/1 Details

    omeprazole 20 mg/1

    omeprazole is a ORAL TABLET, DELAYED RELEASE in the HUMAN OTC DRUG category. It is labeled and distributed by THIRTY MADISON INC. The primary component is OMEPRAZOLE.

    Product Information

    NDC 71713-0301
    Product ID 71713-301_98b38ae5-ed68-4ad3-8ea5-4a2753ab19e2
    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
    Proprietary Name Suffix n/a
    Non-Proprietary Name Omeprazole
    Product Type HUMAN OTC DRUG
    Dosage Form TABLET, DELAYED RELEASE
    Route ORAL
    Active Ingredient Strength 20
    Active Ingredient Units mg/1
    Substance Name OMEPRAZOLE
    Labeler Name THIRTY MADISON INC
    Pharmaceutical Class Cytochrome P450 2C19 Inhibitors [MoA], Proton Pump Inhibitor [EPC], Proton Pump Inhibitors [MoA]
    DEA Schedule n/a
    Marketing Category NDA
    Application Number NDA022032
    Listing Certified Through 2024-12-31

    Package

    NDC 71713-0301-01 (71713030101)

    NDC Package Code 71713-301-01
    Billing NDC 71713030101
    Package 3 BOTTLE in 1 CARTON (71713-301-01) / 14 TABLET, DELAYED RELEASE in 1 BOTTLE
    Marketing Start Date 2022-01-11
    NDC Exclude Flag N
    Pricing Information N/A

    Standard Product Labeling (SPL)/Prescribing Information SPL ba28bd02-ebaf-4062-951f-760d31bd4c50 Details

    Revised: 1/2022