NDC 71335-0785

bupropion

Bupropion Hydrochloride

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

Product ID71335-0785_1d654c22-d2b9-429c-91cb-686249973287
NDC71335-0785
Product TypeHuman Prescription Drug
Proprietary Namebupropion
Generic NameBupropion Hydrochloride
Dosage FormTablet, Extended Release
Route of AdministrationORAL
Marketing Start Date2014-11-01
Marketing CategoryANDA / ANDA
Application NumberANDA202304
Labeler NameBryant Ranch Prepack
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 Through2023-12-31

Packaging

NDC 71335-0785-1

60 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-0785-1)
Marketing Start Date2018-04-18
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 71335-0785-1 [71335078501]

bupropion TABLET, EXTENDED RELEASE
Marketing CategoryANDA
Application NumberANDA202304
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2014-11-01
Marketing End Date2019-09-30

NDC 71335-0785-6 [71335078506]

bupropion TABLET, EXTENDED RELEASE
Marketing CategoryANDA
Application NumberANDA202304
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2014-11-01
Marketing End Date2019-09-30

NDC 71335-0785-4 [71335078504]

bupropion TABLET, EXTENDED RELEASE
Marketing CategoryANDA
Application NumberANDA202304
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2014-11-01
Marketing End Date2019-09-30

NDC 71335-0785-2 [71335078502]

bupropion TABLET, EXTENDED RELEASE
Marketing CategoryANDA
Application NumberANDA202304
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2014-11-01
Marketing End Date2019-09-30

NDC 71335-0785-7 [71335078507]

bupropion TABLET, EXTENDED RELEASE
Marketing CategoryANDA
Application NumberANDA202304
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2014-11-01
Marketing End Date2019-09-30

NDC 71335-0785-3 [71335078503]

bupropion TABLET, EXTENDED RELEASE
Marketing CategoryANDA
Application NumberANDA202304
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2014-11-01
Marketing End Date2019-09-30

NDC 71335-0785-5 [71335078505]

bupropion TABLET, EXTENDED RELEASE
Marketing CategoryANDA
Application NumberANDA202304
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2014-11-01
Marketing End Date2019-09-30

Drug Details

Active Ingredients

IngredientStrength
BUPROPION HYDROCHLORIDE150 mg/1

OpenFDA Data

SPL SET ID:732690c9-eb8a-47a9-9cba-15d07df4e340
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 993518
  • 993536
  • 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" or generic name "Bupropion Hydrochloride"

    NDCBrand NameGeneric Name
    68001-264bupropionbupropion
    68382-353bupropionbupropion
    68382-354bupropionbupropion
    68788-7249bupropionbupropion
    68788-9255bupropionbupropion
    70518-1644bupropionbupropion
    71335-0801bupropionbupropion
    71335-0785bupropionbupropion
    0615-8262bupropionbupropion
    43547-288bupropionbupropion
    43547-289bupropionbupropion
    43547-290bupropionbupropion
    50090-3854bupropionbupropion
    50436-0289bupropionbupropion
    55700-644bupropionbupropion
    63187-521bupropionbupropion
    65841-780bupropionbupropion
    65841-836bupropionbupropion
    70934-151bupropionbupropion
    63629-8036bupropionbupropion
    68788-7283bupropionbupropion
    68071-5214bupropionbupropion
    70518-2641bupropionbupropion
    51655-357bupropionbupropion
    71335-1622bupropionbupropion
    0115-5445Bupropion HydrochlorideBUPROPION HYDROCHLORIDE
    0115-6811Bupropion HydrochlorideBUPROPION HYDROCHLORIDE
    0185-0410Bupropion HydrochlorideBupropion Hydrochloride
    0185-0415Bupropion HydrochlorideBupropion Hydrochloride
    0185-1111Bupropion HydrochlorideBupropion Hydrochloride
    0173-0135WELLBUTRINbupropion hydrochloride
    0173-0722WELLBUTRINbupropion hydrochloride
    0173-0947WELLBUTRINbupropion hydrochloride
    0173-0556ZYBANbupropion hydrochloride

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