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    NDC 72789-0049-90 oxybutynin chloride 10 mg/1 Details

    oxybutynin chloride 10 mg/1

    oxybutynin chloride is a ORAL TABLET, EXTENDED RELEASE in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by PD-Rx Pharmaceuticals, Inc.. The primary component is OXYBUTYNIN CHLORIDE.

    Product Information

    NDC 72789-0049
    Product ID 72789-049_fe464b9c-f4af-0f7d-e053-6394a90a6dcb
    Associated GPIs 54100045207530
    GCN Sequence Number 041047
    GCN Sequence Number Description oxybutynin chloride TAB ER 24 10 MG ORAL
    HIC3 R1A
    HIC3 Description URINARY TRACT ANTISPASMODIC/ANTIINCONTINENCE AGENT
    GCN 19389
    HICL Sequence Number 002048
    HICL Sequence Number Description OXYBUTYNIN CHLORIDE
    Brand/Generic Generic
    Proprietary Name oxybutynin chloride
    Proprietary Name Suffix n/a
    Non-Proprietary Name oxybutynin chloride
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET, EXTENDED RELEASE
    Route ORAL
    Active Ingredient Strength 10
    Active Ingredient Units mg/1
    Substance Name OXYBUTYNIN CHLORIDE
    Labeler Name PD-Rx Pharmaceuticals, Inc.
    Pharmaceutical Class Cholinergic Muscarinic Antagonist [EPC], Cholinergic Muscarinic Antagonists [MoA]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA207138
    Listing Certified Through 2024-12-31

    Package

    NDC 72789-0049-90 (72789004990)

    NDC Package Code 72789-049-90
    Billing NDC 72789004990
    Package 90 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (72789-049-90)
    Marketing Start Date 2020-01-28
    NDC Exclude Flag N
    Pricing Information N/A