NDC 71335-0006

BUPROPION HYDROCHLORIDE (SR)

Bupropion Hydrochloride

BUPROPION HYDROCHLORIDE (SR) 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 ID71335-0006_098f9320-427d-494c-84ae-557715100cf2
NDC71335-0006
Product TypeHuman Prescription Drug
Proprietary NameBUPROPION HYDROCHLORIDE (SR)
Generic NameBupropion Hydrochloride
Dosage FormTablet, Extended Release
Route of AdministrationORAL
Marketing Start Date2016-07-25
Marketing CategoryANDA / ANDA
Application NumberANDA206674
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 Through2020-12-31

Packaging

NDC 71335-0006-1

60 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-0006-1)
Marketing Start Date2017-10-09
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 71335-0006-6 [71335000606]

BUPROPION HYDROCHLORIDE (SR) TABLET, EXTENDED RELEASE
Marketing CategoryANDA
Application NumberANDA206674
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2017-10-09

NDC 71335-0006-3 [71335000603]

BUPROPION HYDROCHLORIDE (SR) TABLET, EXTENDED RELEASE
Marketing CategoryANDA
Application NumberANDA206674
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2017-10-09

NDC 71335-0006-2 [71335000602]

BUPROPION HYDROCHLORIDE (SR) TABLET, EXTENDED RELEASE
Marketing CategoryANDA
Application NumberANDA206674
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2017-10-09

NDC 71335-0006-8 [71335000608]

BUPROPION HYDROCHLORIDE (SR) TABLET, EXTENDED RELEASE
Marketing CategoryANDA
Application NumberANDA206674
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2017-10-09

NDC 71335-0006-7 [71335000607]

BUPROPION HYDROCHLORIDE (SR) TABLET, EXTENDED RELEASE
Marketing CategoryANDA
Application NumberANDA206674
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2017-10-09

NDC 71335-0006-5 [71335000605]

BUPROPION HYDROCHLORIDE (SR) TABLET, EXTENDED RELEASE
Marketing CategoryANDA
Application NumberANDA206674
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2017-10-09

NDC 71335-0006-1 [71335000601]

BUPROPION HYDROCHLORIDE (SR) TABLET, EXTENDED RELEASE
Marketing CategoryANDA
Application NumberANDA206674
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2017-10-09

NDC 71335-0006-4 [71335000604]

BUPROPION HYDROCHLORIDE (SR) TABLET, EXTENDED RELEASE
Marketing CategoryANDA
Application NumberANDA206674
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2017-10-09

Drug Details

Active Ingredients

IngredientStrength
BUPROPION HYDROCHLORIDE150 mg/1

OpenFDA Data

SPL SET ID:9643e5d8-5c59-4d2e-b4a5-12b50f672b19
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 HYDROCHLORIDE (SR)" or generic name "Bupropion Hydrochloride"

    NDCBrand NameGeneric Name
    69097-879BUPROPION HYDROCHLORIDE (SR)BUPROPION HYDROCHLORIDE (SR)
    69097-878BUPROPION HYDROCHLORIDE (SR)BUPROPION HYDROCHLORIDE (SR)
    69097-877BUPROPION HYDROCHLORIDE (SR)BUPROPION HYDROCHLORIDE (SR)
    70518-1033BUPROPION HYDROCHLORIDE (SR)BUPROPION HYDROCHLORIDE (SR)
    70934-156BUPROPION HYDROCHLORIDE (SR)BUPROPION HYDROCHLORIDE (SR)
    71335-0006BUPROPION HYDROCHLORIDE (SR)BUPROPION HYDROCHLORIDE (SR)
    71335-0025BUPROPION HYDROCHLORIDE (SR)BUPROPION HYDROCHLORIDE (SR)
    45865-633BUPROPION HYDROCHLORIDE (SR)BUPROPION HYDROCHLORIDE (SR)
    50090-3453BUPROPION HYDROCHLORIDE (SR)BUPROPION HYDROCHLORIDE (SR)
    50090-3249BUPROPION HYDROCHLORIDE (SR)BUPROPION HYDROCHLORIDE (SR)
    53002-1509BUPROPION HYDROCHLORIDE (SR)BUPROPION HYDROCHLORIDE (SR)
    55648-107Bupropion Hydrochloride (SR)Bupropion Hydrochloride (SR)
    55648-105Bupropion Hydrochloride (SR)Bupropion Hydrochloride (SR)
    55648-101Bupropion Hydrochloride (SR)Bupropion Hydrochloride (SR)
    58118-0878BUPROPION HYDROCHLORIDE (SR)BUPROPION HYDROCHLORIDE (SR)
    64679-105Bupropion Hydrochloride (SR)Bupropion Hydrochloride (SR)
    64679-101Bupropion Hydrochloride (SR)Bupropion Hydrochloride (SR)
    64679-107Bupropion Hydrochloride (SR)Bupropion Hydrochloride (SR)
    43598-863BUPROPION HYDROCHLORIDE (SR)BUPROPION HYDROCHLORIDE (SR)
    50228-338Bupropion Hydrochloride (SR)Bupropion Hydrochloride (SR)
    70518-2648BUPROPION HYDROCHLORIDE (SR)BUPROPION HYDROCHLORIDE (SR)
    50090-5101BUPROPION HYDROCHLORIDE (SR)BUPROPION HYDROCHLORIDE (SR)
    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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