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    NDC 69117-0043-02 Buspirone hydrochloride 30 mg/1 Details

    Buspirone hydrochloride 30 mg/1

    Buspirone hydrochloride is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Yiling Pharmaceutical, Inc.. The primary component is BUSPIRONE HYDROCHLORIDE.

    Product Information

    NDC 69117-0043
    Product ID 69117-0043_f16635a5-7e1a-534a-e053-2995a90a9355
    Associated GPIs 57200005100340
    GCN Sequence Number 044210
    GCN Sequence Number Description buspirone HCl TABLET 30 MG ORAL
    HIC3 H2F
    HIC3 Description ANTI-ANXIETY DRUGS
    GCN 92121
    HICL Sequence Number 001620
    HICL Sequence Number Description BUSPIRONE HCL
    Brand/Generic Generic
    Proprietary Name Buspirone hydrochloride
    Proprietary Name Suffix n/a
    Non-Proprietary Name Buspirone hydrochloride
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET
    Route ORAL
    Active Ingredient Strength 30
    Active Ingredient Units mg/1
    Substance Name BUSPIRONE HYDROCHLORIDE
    Labeler Name Yiling Pharmaceutical, Inc.
    Pharmaceutical Class n/a
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA202087
    Listing Certified Through 2024-12-31

    Package

    NDC 69117-0043-02 (69117004302)

    NDC Package Code 69117-0043-2
    Billing NDC 69117004302
    Package 500 TABLET in 1 BOTTLE (69117-0043-2)
    Marketing Start Date 2019-10-30
    NDC Exclude Flag N
    Pricing Information N/A