NDC 71335-1192

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 ID71335-1192_2f5e0c2f-1de7-48d7-9088-8a395bdffba0
NDC71335-1192
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 Strength100 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 71335-1192-1

60 TABLET in 1 BOTTLE (71335-1192-1)
Marketing Start Date2019-04-22
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 71335-1192-6 [71335119206]

bupropion Hydrochloride TABLET
Marketing CategoryANDA
Application NumberANDA206975
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2019-04-22

NDC 71335-1192-1 [71335119201]

bupropion Hydrochloride TABLET
Marketing CategoryANDA
Application NumberANDA206975
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2019-04-22

NDC 71335-1192-3 [71335119203]

bupropion Hydrochloride TABLET
Marketing CategoryANDA
Application NumberANDA206975
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2019-04-22

NDC 71335-1192-2 [71335119202]

bupropion Hydrochloride TABLET
Marketing CategoryANDA
Application NumberANDA206975
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2019-04-22

NDC 71335-1192-5 [71335119205]

bupropion Hydrochloride TABLET
Marketing CategoryANDA
Application NumberANDA206975
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2019-04-22

NDC 71335-1192-4 [71335119204]

bupropion Hydrochloride TABLET
Marketing CategoryANDA
Application NumberANDA206975
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2019-04-22

Drug Details

Active Ingredients

IngredientStrength
BUPROPION HYDROCHLORIDE100 mg/1

OpenFDA Data

SPL SET ID:144379e1-93b7-41c1-bc3a-7bdec5afa309
Manufacturer
UNII

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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