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    NDC 55154-7986-00 Bupropion Hydrochloride 150 mg/1 Details

    Bupropion Hydrochloride 150 mg/1

    Bupropion Hydrochloride is a ORAL TABLET, EXTENDED RELEASE in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Cardinal Health 107, LLC. The primary component is BUPROPION HYDROCHLORIDE.

    Product Information

    NDC 55154-7986
    Product ID 55154-7986_867a28c5-dcad-4614-971b-4c72034b83be
    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 Bupropion Hydrochloride
    Proprietary Name Suffix n/a
    Non-Proprietary Name Bupropion Hydrochloride
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET, EXTENDED RELEASE
    Route ORAL
    Active Ingredient Strength 150
    Active Ingredient Units mg/1
    Substance Name BUPROPION HYDROCHLORIDE
    Labeler Name Cardinal Health 107, LLC
    Pharmaceutical Class Aminoketone [EPC], Dopamine Uptake Inhibitors [MoA], Increased Dopamine Activity [PE], Increased Norepinephrine Activity [PE], Norepinephrine Uptake Inhibitors [MoA]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA075932
    Listing Certified Through 2023-12-31

    Package

    NDC 55154-7986-00 (55154798600)

    NDC Package Code 55154-7986-0
    Billing NDC 55154798600
    Package 10 BLISTER PACK in 1 BAG (55154-7986-0) / 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK
    Marketing Start Date 2004-03-22
    NDC Exclude Flag N
    Pricing Information N/A