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    NDC 71335-0974-04 oxybutynin 10 mg/1 Details

    oxybutynin 10 mg/1

    oxybutynin is a ORAL TABLET, FILM COATED, EXTENDED RELEASE in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Bryant Ranch Prepack. The primary component is OXYBUTYNIN CHLORIDE.

    Product Information

    NDC 71335-0974
    Product ID 71335-0974_d2d70788-5d53-4e4e-aaa6-5ca7ab0cb759
    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 oxybutynin
    Proprietary Name Suffix n/a
    Non-Proprietary Name oxybutynin
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET, FILM COATED, EXTENDED RELEASE
    Route ORAL
    Active Ingredient Strength 10
    Active Ingredient Units mg/1
    Substance Name OXYBUTYNIN CHLORIDE
    Labeler Name Bryant Ranch Prepack
    Pharmaceutical Class Cholinergic Muscarinic Antagonist [EPC], Cholinergic Muscarinic Antagonists [MoA]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA202332
    Listing Certified Through 2023-12-31

    Package

    NDC 71335-0974-04 (71335097404)

    NDC Package Code 71335-0974-4
    Billing NDC 71335097404
    Package 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-0974-4)
    Marketing Start Date 2021-12-28
    NDC Exclude Flag N
    Pricing Information N/A