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    NDC 68788-7793-06 Bupropion Hydrochloride 200 mg/1 Details

    Bupropion Hydrochloride 200 mg/1

    Bupropion Hydrochloride is a ORAL TABLET, FILM COATED, EXTENDED RELEASE in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Preferred Pharmaceuticals, Inc.. The primary component is BUPROPION HYDROCHLORIDE.

    Product Information

    NDC 68788-7793
    Product ID 68788-7793_c9bccbb5-ec25-477b-b676-ee26da6b8e6e
    Associated GPIs 58300040107440
    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 SR
    Non-Proprietary Name bupropion hydrochloride
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET, FILM COATED, EXTENDED RELEASE
    Route ORAL
    Active Ingredient Strength 200
    Active Ingredient Units mg/1
    Substance Name BUPROPION HYDROCHLORIDE
    Labeler Name Preferred Pharmaceuticals, Inc.
    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 ANDA205794
    Listing Certified Through 2024-12-31

    Package

    NDC 68788-7793-06 (68788779306)

    NDC Package Code 68788-7793-6
    Billing NDC 68788779306
    Package 60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (68788-7793-6)
    Marketing Start Date 2020-10-13
    NDC Exclude Flag N
    Pricing Information N/A