Search by Drug Name or NDC

    NDC 71335-0552-02 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 Bryant Ranch Prepack. The primary component is BUSPIRONE HYDROCHLORIDE.

    Product Information

    NDC 71335-0552
    Product ID 71335-0552_cd86018f-fc93-45d7-88a6-7f7fa0cee810
    Associated GPIs 57200005100340
    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 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 Bryant Ranch Prepack
    Pharmaceutical Class n/a
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA078888
    Listing Certified Through 2023-12-31

    Package

    NDC 71335-0552-02 (71335055202)

    NDC Package Code 71335-0552-2
    Billing NDC 71335055202
    Package 30 TABLET in 1 BLISTER PACK (71335-0552-2)
    Marketing Start Date 2022-02-09
    NDC Exclude Flag N
    Pricing Information N/A