NDC 71335-0791

bupropion Hydrochloride

Bupropion Hydrochloride

bupropion Hydrochloride is a Oral Tablet in the Human Prescription Drug category. It is labeled and distributed by Bryant Ranch Prepack. The primary component is Bupropion Hydrochloride.

Product ID71335-0791_144379e1-93b7-41c1-bc3a-7bdec5afa309
NDC71335-0791
Product TypeHuman Prescription Drug
Proprietary Namebupropion Hydrochloride
Generic NameBupropion Hydrochloride
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2016-08-19
Marketing CategoryANDA / ANDA
Application NumberANDA206975
Labeler NameBryant Ranch Prepack
Substance NameBUPROPION HYDROCHLORIDE
Active Ingredient Strength75 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 Through2023-12-31

Packaging

NDC 71335-0791-1

30 TABLET in 1 BOTTLE (71335-0791-1)
Marketing Start Date2018-04-26
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 71335-0791-1 [71335079101]

bupropion Hydrochloride TABLET
Marketing CategoryANDA
Application NumberANDA206975
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2018-04-30
Marketing End Date2019-09-30

NDC 71335-0791-4 [71335079104]

bupropion Hydrochloride TABLET
Marketing CategoryANDA
Application NumberANDA206975
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2018-04-30
Marketing End Date2019-09-30

NDC 71335-0791-7 [71335079107]

bupropion Hydrochloride TABLET
Marketing CategoryANDA
Application NumberANDA206975
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2018-04-30
Marketing End Date2019-09-30

NDC 71335-0791-2 [71335079102]

bupropion Hydrochloride TABLET
Marketing CategoryANDA
Application NumberANDA206975
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2018-04-30
Marketing End Date2019-09-30

NDC 71335-0791-6 [71335079106]

bupropion Hydrochloride TABLET
Marketing CategoryANDA
Application NumberANDA206975
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2018-04-30
Marketing End Date2019-09-30

NDC 71335-0791-3 [71335079103]

bupropion Hydrochloride TABLET
Marketing CategoryANDA
Application NumberANDA206975
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2018-04-30
Marketing End Date2019-09-30

NDC 71335-0791-5 [71335079105]

bupropion Hydrochloride TABLET
Marketing CategoryANDA
Application NumberANDA206975
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2018-04-30
Marketing End Date2019-09-30

Drug Details

Active Ingredients

IngredientStrength
BUPROPION HYDROCHLORIDE75 mg/1

OpenFDA Data

SPL SET ID:144379e1-93b7-41c1-bc3a-7bdec5afa309
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 993691
  • 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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