NDC 63629-7033

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 Bryant Ranch Prepack. The primary component is Bupropion Hydrochloride.

Product ID63629-7033_429047a2-c10f-4001-8e25-112091fb7c0e
NDC63629-7033
Product TypeHuman Prescription Drug
Proprietary NameBupropion Hydrochloride
Generic NameBupropion Hydrochloride
Dosage FormTablet, Film Coated, Extended Release
Route of AdministrationORAL
Marketing Start Date2009-05-01
Marketing CategoryANDA / ANDA
Application NumberANDA077415
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 Through2021-12-31

Packaging

NDC 63629-7033-1

30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63629-7033-1)
Marketing Start Date2016-07-07
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 63629-7033-1 [63629703301]

Bupropion Hydrochloride TABLET, FILM COATED, EXTENDED RELEASE
Marketing CategoryANDA
Application NumberANDA077415
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2018-06-30
Marketing End Date2018-06-30

NDC 63629-7033-4 [63629703304]

Bupropion Hydrochloride TABLET, FILM COATED, EXTENDED RELEASE
Marketing CategoryANDA
Application NumberANDA077415
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2018-06-30
Marketing End Date2018-06-30

NDC 63629-7033-3 [63629703303]

Bupropion Hydrochloride TABLET, FILM COATED, EXTENDED RELEASE
Marketing CategoryANDA
Application NumberANDA077415
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2018-06-30
Marketing End Date2018-06-30

NDC 63629-7033-5 [63629703305]

Bupropion Hydrochloride TABLET, FILM COATED, EXTENDED RELEASE
Marketing CategoryANDA
Application NumberANDA077415
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2018-06-30
Marketing End Date2018-06-30

NDC 63629-7033-2 [63629703302]

Bupropion Hydrochloride TABLET, FILM COATED, EXTENDED RELEASE
Marketing CategoryANDA
Application NumberANDA077415
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2018-06-30
Marketing End Date2018-06-30

NDC 63629-7033-6 [63629703306]

Bupropion Hydrochloride TABLET, FILM COATED, EXTENDED RELEASE
Marketing CategoryANDA
Application NumberANDA077415
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2018-06-30
Marketing End Date2018-06-30

Drug Details

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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