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    NDC 68788-7785-06 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 68788-7785
    Product ID 68788-7785_1e9349c6-bff5-422d-b826-a0b0a103e9f9
    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 ANDA211062
    Listing Certified Through 2024-12-31

    Package

    NDC 68788-7785-06 (68788778506)

    NDC Package Code 68788-7785-6
    Billing NDC 68788778506
    Package 60 TABLET in 1 BOTTLE (68788-7785-6)
    Marketing Start Date 2020-10-20
    NDC Exclude Flag N
    Pricing Information N/A