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    NDC 00065-8150-03 PATADAY ONCE DAILY RELIEF 2 mg/mL Details

    PATADAY ONCE DAILY RELIEF 2 mg/mL

    PATADAY ONCE DAILY RELIEF is a OPHTHALMIC SOLUTION in the HUMAN OTC DRUG category. It is labeled and distributed by Alcon Laboratories, Inc.. The primary component is OLOPATADINE HYDROCHLORIDE.

    Product Information

    NDC 00065-8150
    Product ID 0065-8150_30e4fc2d-7d06-477a-9160-aa231b83e642
    Associated GPIs 86802065102030
    GCN Sequence Number 062065
    GCN Sequence Number Description olopatadine HCl DROPS 0.2 % OPHTHALMIC
    HIC3 Q6R
    HIC3 Description EYE ANTIHISTAMINES
    GCN 97848
    HICL Sequence Number 012815
    HICL Sequence Number Description OLOPATADINE HCL
    Brand/Generic Brand
    Proprietary Name PATADAY ONCE DAILY RELIEF
    Proprietary Name Suffix n/a
    Non-Proprietary Name OLOPATADINE HYDROCHLORIDE
    Product Type HUMAN OTC DRUG
    Dosage Form SOLUTION
    Route OPHTHALMIC
    Active Ingredient Strength 2
    Active Ingredient Units mg/mL
    Substance Name OLOPATADINE HYDROCHLORIDE
    Labeler Name Alcon Laboratories, Inc.
    Pharmaceutical Class Decreased Histamine Release [PE], Histamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC], Histamine-1 Receptor Inhibitor [EPC], Mast Cell Stabilizer [EPC]
    DEA Schedule n/a
    Marketing Category NDA
    Application Number NDA021545
    Listing Certified Through 2024-12-31

    Package

    NDC 00065-8150-03 (00065815003)

    NDC Package Code 0065-8150-03
    Billing NDC 00065815003
    Package 2 BOTTLE, PLASTIC in 1 CARTON (0065-8150-03) / 2.5 mL in 1 BOTTLE, PLASTIC
    Marketing Start Date 2020-02-28
    NDC Exclude Flag N
    Pricing Information N/A