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    NDC 68788-8141-09 Oxybutynin Chloride 5 mg/1 Details

    Oxybutynin Chloride 5 mg/1

    Oxybutynin Chloride is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Preferred Pharmaceuticals Inc.. The primary component is OXYBUTYNIN CHLORIDE.

    Product Information

    NDC 68788-8141
    Product ID 68788-8141_6c540df9-b063-46c7-9321-763225b8f3d3
    Associated GPIs 54100045200330
    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 Oxybutynin Chloride
    Proprietary Name Suffix n/a
    Non-Proprietary Name Oxybutynin Chloride
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET
    Route ORAL
    Active Ingredient Strength 5
    Active Ingredient Units mg/1
    Substance Name OXYBUTYNIN CHLORIDE
    Labeler Name Preferred Pharmaceuticals Inc.
    Pharmaceutical Class Cholinergic Muscarinic Antagonist [EPC], Cholinergic Muscarinic Antagonists [MoA]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA209335
    Listing Certified Through 2024-12-31

    Package

    NDC 68788-8141-09 (68788814109)

    NDC Package Code 68788-8141-9
    Billing NDC 68788814109
    Package 90 TABLET in 1 BOTTLE, PLASTIC (68788-8141-9)
    Marketing Start Date 2022-02-11
    NDC Exclude Flag N
    Pricing Information N/A