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    NDC 68788-7786-08 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 Preferred Pharmaceuticals Inc.. The primary component is BUPROPION HYDROCHLORIDE.

    Product Information

    NDC 68788-7786
    Product ID 68788-7786_e7f0f983-b361-4a18-be5a-9a8bcb88a36b
    Associated GPIs 58300040107520
    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 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 ANDA210497
    Listing Certified Through 2024-12-31

    Package

    NDC 68788-7786-08 (68788778608)

    NDC Package Code 68788-7786-8
    Billing NDC 68788778608
    Package 120 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-7786-8)
    Marketing Start Date 2020-10-21
    NDC Exclude Flag N
    Pricing Information N/A