NDC 68788-6800

Bupropion Hydrochloride

Bupropion Hydrochloride

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 ID68788-6800_1b3e1a5b-65e9-4b5d-83a5-b738ade6b370
NDC68788-6800
Product TypeHuman Prescription Drug
Proprietary NameBupropion Hydrochloride
Generic NameBupropion Hydrochloride
Dosage FormTablet, Film Coated, Extended Release
Route of AdministrationORAL
Marketing Start Date2016-10-31
Marketing CategoryANDA / ANDA
Application NumberANDA077415
Labeler NamePreferred Pharmaceuticals, Inc.
Substance NameBUPROPION HYDROCHLORIDE
Active Ingredient Strength150 mg/1
Pharm ClassesAminoketone [EPC],Dopamine Uptake Inhibitors [MoA],Increased Dopamine Activity [PE],Increased Norepinephrine Activity [PE],Norepinephrine Uptake Inhibitors [MoA]
NDC Exclude FlagN
Listing Certified Through2021-12-31

Packaging

NDC 68788-6800-1

100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (68788-6800-1)
Marketing Start Date2016-10-31
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 68788-6800-3 [68788680003]

Bupropion Hydrochloride TABLET, FILM COATED, EXTENDED RELEASE
Marketing CategoryANDA
Application NumberANDA077415
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2016-10-31

NDC 68788-6800-9 [68788680009]

Bupropion Hydrochloride TABLET, FILM COATED, EXTENDED RELEASE
Marketing CategoryANDA
Application NumberANDA077415
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2016-10-31

NDC 68788-6800-6 [68788680006]

Bupropion Hydrochloride TABLET, FILM COATED, EXTENDED RELEASE
Marketing CategoryANDA
Application NumberANDA077415
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2016-10-31

NDC 68788-6800-8 [68788680008]

Bupropion Hydrochloride TABLET, FILM COATED, EXTENDED RELEASE
Marketing CategoryANDA
Application NumberANDA077415
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2016-10-31

NDC 68788-6800-1 [68788680001]

Bupropion Hydrochloride TABLET, FILM COATED, EXTENDED RELEASE
Marketing CategoryANDA
Application NumberANDA077415
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2016-10-31

Drug Details

Active Ingredients

IngredientStrength
BUPROPION HYDROCHLORIDE150 mg/1

OpenFDA Data

SPL SET ID:63f1d462-6b26-4759-8069-5425bdeee2aa
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 993541

    • Pharmacological Class

    • Aminoketone [EPC]
    • Dopamine Uptake Inhibitors [MoA]
    • Increased Dopamine Activity [PE]
    • Increased Norepinephrine Activity [PE]
    • Norepinephrine Uptake Inhibitors [MoA]

    NDC Crossover Matching brand name "Bupropion Hydrochloride" or generic name "Bupropion Hydrochloride"

    NDCBrand NameGeneric Name
    0115-5445Bupropion HydrochlorideBUPROPION HYDROCHLORIDE
    0115-6811Bupropion HydrochlorideBUPROPION HYDROCHLORIDE
    0185-0410Bupropion HydrochlorideBupropion Hydrochloride
    0185-0415Bupropion HydrochlorideBupropion Hydrochloride
    0185-1111Bupropion HydrochlorideBupropion Hydrochloride
    67544-892Bupropion HydrochlorideBupropion Hydrochloride
    68001-199Bupropion HydrochlorideBupropion Hydrochloride
    68001-198Bupropion HydrochlorideBupropion Hydrochloride
    68001-309Bupropion HydrochlorideBupropion Hydrochloride
    68001-308Bupropion HydrochlorideBupropion Hydrochloride
    68084-252Bupropion HydrochlorideBupropion Hydrochloride
    0440-7200Bupropion HydrochlorideBupropion Hydrochloride
    68084-697BuPROPion HydrochlorideBuPROPion Hydrochloride
    68084-708Bupropion HydrochlorideBupropion Hydrochloride
    68180-319Bupropion HydrochlorideBupropion Hydrochloride
    68180-320Bupropion HydrochlorideBupropion Hydrochloride
    68258-7157Bupropion hydrochlorideBupropion hydrochloride
    68258-7001Bupropion HydrochlorideBupropion Hydrochloride
    68788-6800Bupropion HydrochlorideBupropion Hydrochloride
    68788-6994Bupropion HydrochlorideBupropion Hydrochloride
    68788-6808Bupropion HydrochlorideBupropion Hydrochloride
    68788-7121Bupropion HydrochlorideBupropion Hydrochloride
    68788-7319bupropion Hydrochloridebupropion Hydrochloride
    68788-7170Bupropion HydrochlorideBupropion Hydrochloride
    68788-7221Bupropion HydrochlorideBupropion Hydrochloride
    68788-9781Bupropion HydrochlorideBupropion Hydrochloride
    68788-9524Bupropion HydrochlorideBupropion Hydrochloride
    69097-917bupropion Hydrochloridebupropion Hydrochloride
    69097-918bupropion Hydrochloridebupropion Hydrochloride
    69844-010bupropion hydrochloridebupropion hydrochloride
    69844-011bupropion hydrochloridebupropion hydrochloride
    70518-0414Bupropion HydrochlorideBupropion Hydrochloride
    70518-0227Bupropion HydrochlorideBupropion Hydrochloride
    70518-0897Bupropion HydrochlorideBupropion Hydrochloride
    70518-0900Bupropion HydrochlorideBupropion Hydrochloride
    70518-0788Bupropion HydrochlorideBupropion Hydrochloride
    70518-0349Bupropion HydrochlorideBupropion Hydrochloride
    70518-1437Bupropion HydrochlorideBupropion Hydrochloride
    70518-1189Bupropion HydrochlorideBupropion Hydrochloride
    70518-1468Bupropion HydrochlorideBupropion Hydrochloride
    70518-1566Bupropion HydrochlorideBupropion Hydrochloride
    70518-1584Bupropion HydrochlorideBupropion Hydrochloride
    70518-0859Bupropion HydrochlorideBupropion Hydrochloride
    70518-1711Bupropion HydrochlorideBupropion Hydrochloride
    71335-0013Bupropion HydrochlorideBupropion Hydrochloride
    71335-0019Bupropion HydrochlorideBupropion Hydrochloride
    71335-0331Bupropion HydrochlorideBupropion Hydrochloride
    71335-0502Bupropion HydrochlorideBupropion Hydrochloride
    71335-0687Bupropion HydrochlorideBupropion Hydrochloride
    71335-0791bupropion Hydrochloridebupropion Hydrochloride
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