NDC 42291-182

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 Avkare, Inc.. The primary component is Bupropion Hydrochloride.

• Product ID: 42291-182_7b08df3e-ee1f-03d7-e053-2a91aa0a251b
• NDC: 42291-182
• Product Type: Human Prescription Drug
• Proprietary Name: Bupropion Hydrochloride
• Generic Name: Bupropion Hydrochloride
• Dosage Form: Tablet, Film Coated, Extended Release
• Route of Administration: ORAL
• Marketing Start Date: 2016-01-27
• Marketing Category: ANDA / ANDA
• Application Number: ANDA077284
• Labeler Name: AvKARE, Inc.
• Substance Name: BUPROPION HYDROCHLORIDE
• Active Ingredient Strength: 150 mg/1
• Pharm Classes: Aminoketone [EPC],Dopamine Uptake Inhibitors [MoA],Increased Dopamine Activity [PE],Increased Norepinephrine Activity [PE],Norepinephrine Uptake Inhibitors [MoA]
• NDC Exclude Flag: N
• Listing Certified Through: 2020-12-31

Packaging

NDC 42291-182-30

30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (42291-182-30)

• Marketing Start Date: 2022-11-16
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 42291-182-30 [42291018230]

Bupropion Hydrochloride TABLET, FILM COATED, EXTENDED RELEASE

• Marketing Category: ANDA
• Application Number: ANDA077284
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: EA
• Marketing Start Date: 2016-01-27
• Marketing End Date: 2018-10-31

NDC 42291-182-90 [42291018290]

Bupropion Hydrochloride TABLET, FILM COATED, EXTENDED RELEASE

• Marketing Category: ANDA
• Application Number: ANDA077284
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: EA
• Marketing Start Date: 2016-01-27
• Marketing End Date: 2018-10-31

NDC 42291-182-50 [42291018250]

Bupropion Hydrochloride TABLET, FILM COATED, EXTENDED RELEASE

• Marketing Category: ANDA
• Application Number: ANDA077284
• Product Type: HUMAN PRESCRIPTION DRUG
• Billing Unit: EA
• Marketing Start Date: 2016-01-27
• Marketing End Date: 2020-02-03

Drug Details

Active Ingredients

Ingredient	Strength
BUPROPION HYDROCHLORIDE	150 mg/1

OpenFDA Data

• SPL SET ID: 6cbcff19-39b1-c833-911a-d12b0c174880
• Manufacturer:
  • AvKARE, Inc.
• UNII:
  • ZG7E5POY8O
• RxNorm Concept Unique ID - RxCUI:
  • 993557
  • 993541
• UPC Code:
  • 0342291182301
  • 0342291183308

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"

NDC	Brand Name	Generic Name
0115-5445	Bupropion Hydrochloride	BUPROPION HYDROCHLORIDE
0115-6811	Bupropion Hydrochloride	BUPROPION HYDROCHLORIDE
0185-0410	Bupropion Hydrochloride	Bupropion Hydrochloride
0185-0415	Bupropion Hydrochloride	Bupropion Hydrochloride
0185-1111	Bupropion Hydrochloride	Bupropion Hydrochloride
67544-892	Bupropion Hydrochloride	Bupropion Hydrochloride
68001-199	Bupropion Hydrochloride	Bupropion Hydrochloride
68001-198	Bupropion Hydrochloride	Bupropion Hydrochloride
68001-309	Bupropion Hydrochloride	Bupropion Hydrochloride
68001-308	Bupropion Hydrochloride	Bupropion Hydrochloride
68084-252	Bupropion Hydrochloride	Bupropion Hydrochloride
0440-7200	Bupropion Hydrochloride	Bupropion Hydrochloride
68084-697	BuPROPion Hydrochloride	BuPROPion Hydrochloride
68084-708	Bupropion Hydrochloride	Bupropion Hydrochloride
68180-319	Bupropion Hydrochloride	Bupropion Hydrochloride
68180-320	Bupropion Hydrochloride	Bupropion Hydrochloride
68258-7157	Bupropion hydrochloride	Bupropion hydrochloride
68258-7001	Bupropion Hydrochloride	Bupropion Hydrochloride
68788-6800	Bupropion Hydrochloride	Bupropion Hydrochloride
68788-6994	Bupropion Hydrochloride	Bupropion Hydrochloride
68788-6808	Bupropion Hydrochloride	Bupropion Hydrochloride
68788-7121	Bupropion Hydrochloride	Bupropion Hydrochloride
68788-7319	bupropion Hydrochloride	bupropion Hydrochloride
68788-7170	Bupropion Hydrochloride	Bupropion Hydrochloride
68788-7221	Bupropion Hydrochloride	Bupropion Hydrochloride
68788-9781	Bupropion Hydrochloride	Bupropion Hydrochloride
68788-9524	Bupropion Hydrochloride	Bupropion Hydrochloride
69097-917	bupropion Hydrochloride	bupropion Hydrochloride
69097-918	bupropion Hydrochloride	bupropion Hydrochloride
69844-010	bupropion hydrochloride	bupropion hydrochloride
69844-011	bupropion hydrochloride	bupropion hydrochloride
70518-0414	Bupropion Hydrochloride	Bupropion Hydrochloride
70518-0227	Bupropion Hydrochloride	Bupropion Hydrochloride
70518-0897	Bupropion Hydrochloride	Bupropion Hydrochloride
70518-0900	Bupropion Hydrochloride	Bupropion Hydrochloride
70518-0788	Bupropion Hydrochloride	Bupropion Hydrochloride
70518-0349	Bupropion Hydrochloride	Bupropion Hydrochloride
70518-1437	Bupropion Hydrochloride	Bupropion Hydrochloride
70518-1189	Bupropion Hydrochloride	Bupropion Hydrochloride
70518-1468	Bupropion Hydrochloride	Bupropion Hydrochloride
70518-1566	Bupropion Hydrochloride	Bupropion Hydrochloride
70518-1584	Bupropion Hydrochloride	Bupropion Hydrochloride
70518-0859	Bupropion Hydrochloride	Bupropion Hydrochloride
70518-1711	Bupropion Hydrochloride	Bupropion Hydrochloride
71335-0013	Bupropion Hydrochloride	Bupropion Hydrochloride
71335-0019	Bupropion Hydrochloride	Bupropion Hydrochloride
71335-0331	Bupropion Hydrochloride	Bupropion Hydrochloride
71335-0502	Bupropion Hydrochloride	Bupropion Hydrochloride
71335-0687	Bupropion Hydrochloride	Bupropion Hydrochloride
71335-0791	bupropion Hydrochloride	bupropion Hydrochloride