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    NDC 55700-0779-60 Bupropion Hydrochloride 100 mg/1 Details

    Bupropion Hydrochloride 100 mg/1

    Bupropion Hydrochloride is a ORAL TABLET, FILM COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Quality Care Products, LLC. The primary component is BUPROPION HYDROCHLORIDE.

    Product Information

    NDC 55700-0779
    Product ID 55700-779_577769dc-9077-456f-bd70-17045ea9ec50
    Associated GPIs 58300040100310
    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, FILM COATED
    Route ORAL
    Active Ingredient Strength 100
    Active Ingredient Units mg/1
    Substance Name BUPROPION HYDROCHLORIDE
    Labeler Name Quality Care Products, 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 ANDA076143
    Listing Certified Through 2024-12-31

    Package

    NDC 55700-0779-60 (55700077960)

    NDC Package Code 55700-779-60
    Billing NDC 55700077960
    Package 60 TABLET, FILM COATED in 1 BOTTLE (55700-779-60)
    Marketing Start Date 2019-07-26
    NDC Exclude Flag N
    Pricing Information N/A