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    NDC 60505-6222-03 Olopatadine hydrochloride 2 mg/mL Details

    Olopatadine hydrochloride 2 mg/mL

    Olopatadine hydrochloride is a OPHTHALMIC SOLUTION/ DROPS in the HUMAN OTC DRUG category. It is labeled and distributed by Apotex Corp.. The primary component is OLOPATADINE HYDROCHLORIDE.

    Product Information

    NDC 60505-6222
    Product ID 60505-6222_a5cfb475-5968-b0f0-1772-b6ae0f040898
    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 Olopatadine hydrochloride
    Proprietary Name Suffix n/a
    Non-Proprietary Name Olopatadine hydrochloride
    Product Type HUMAN OTC DRUG
    Dosage Form SOLUTION/ DROPS
    Route OPHTHALMIC
    Active Ingredient Strength 2
    Active Ingredient Units mg/mL
    Substance Name OLOPATADINE HYDROCHLORIDE
    Labeler Name Apotex Corp.
    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 ANDA
    Application Number ANDA090918
    Listing Certified Through 2024-12-31

    Package

    NDC 60505-6222-03 (60505622203)

    NDC Package Code 60505-6222-3
    Billing NDC 60505622203
    Package 2 BOTTLE, PLASTIC in 1 CARTON (60505-6222-3) / 2.5 mL in 1 BOTTLE, PLASTIC
    Marketing Start Date 2022-10-06
    NDC Exclude Flag N
    Pricing Information N/A