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    NDC 51655-0390-25 bupropion Hydrochloride 100 mg/1 Details

    bupropion Hydrochloride 100 mg/1

    bupropion Hydrochloride is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Northwind Pharmaceuticals. The primary component is BUPROPION HYDROCHLORIDE.

    Product Information

    NDC 51655-0390
    Product ID 51655-390_d9bbacb3-63b5-2922-e053-2a95a90a6085
    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
    Route ORAL
    Active Ingredient Strength 100
    Active Ingredient Units mg/1
    Substance Name BUPROPION HYDROCHLORIDE
    Labeler Name Northwind Pharmaceuticals
    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 ANDA206975
    Listing Certified Through 2024-12-31

    Package

    NDC 51655-0390-25 (51655039025)

    NDC Package Code 51655-390-25
    Billing NDC 51655039025
    Package 60 TABLET in 1 BOTTLE, PLASTIC (51655-390-25)
    Marketing Start Date 2022-01-28
    NDC Exclude Flag N
    Pricing Information N/A