Application 018644

Type: NDA
Sponsor: GLAXOSMITHKLINE

Application Products#

Product, Drug, Ingredient table
Product	Drug	Ingredient	Form	Strength	Reference drug	Reference standard
001	WELLBUTRIN	BUPROPION HYDROCHLORIDE	TABLET;ORAL	50MG Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons	Yes	No
002	WELLBUTRIN	BUPROPION HYDROCHLORIDE	TABLET;ORAL	75MG Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons	Yes	No
003	WELLBUTRIN	BUPROPION HYDROCHLORIDE	TABLET;ORAL	100MG Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons	Yes	No

Source provenance: Browse the complete Orange Book source catalog · source snapshot 43.

Orange Book products#

Current product rows page 1 of 1 · 3 matching rows.

Application-product, Trade name, Ingredient table
Application-product	Trade name	Ingredient	Strength	Dosage form / route	RLD / RS	Approval date
N018644-001	WELLBUTRIN	BUPROPION HYDROCHLORIDE	50MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	1985-12-30
N018644-002	WELLBUTRIN	BUPROPION HYDROCHLORIDE	75MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	1985-12-30
N018644-003	WELLBUTRIN	BUPROPION HYDROCHLORIDE	100MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	1985-12-30

Observed Orange Book product history#

Observed FDA ZIP history: Each table is queried independently by exact application/product key from successfully parsed Orange Book snapshots. Capture times identify archived source observations; absence or a change between snapshots is not inferred. FDA publication files that were not recoverable as structured ZIP data are not represented as states.

Product history page 1 of 4 · 129 observed states.

Captured, Edition, Application-product table
Captured	Edition	Application-product	Trade name	Strength	Dosage form / route	RLD / RS	Approval date	Source SHA-256
2026-09-14 22:38:34	2026-08	N018644-001	WELLBUTRIN	50MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	1985-12-30	`84e616aacf4f…`
2026-09-14 22:38:34	2026-08	N018644-002	WELLBUTRIN	75MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	1985-12-30	`84e616aacf4f…`
2026-09-14 22:38:34	2026-08	N018644-003	WELLBUTRIN	100MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	1985-12-30	`84e616aacf4f…`
2026-08-18 06:07:40	2026-07	N018644-001	WELLBUTRIN	50MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	1985-12-30	`caaa826d4ba7…`
2026-08-18 06:07:40	2026-07	N018644-002	WELLBUTRIN	75MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	1985-12-30	`caaa826d4ba7…`
2026-08-18 06:07:40	2026-07	N018644-003	WELLBUTRIN	100MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	1985-12-30	`caaa826d4ba7…`
2026-02-19 14:30 UTC	2026-02	N018644-001	WELLBUTRIN	50MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	1985-12-30	`011fe1cb6892…`
2026-02-19 14:30 UTC	2026-02	N018644-002	WELLBUTRIN	75MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	1985-12-30	`011fe1cb6892…`
2026-02-19 14:30 UTC	2026-02	N018644-003	WELLBUTRIN	100MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	1985-12-30	`011fe1cb6892…`
2025-12-14 10:44 UTC · 2 captures of this ZIP	2025-12	N018644-001	WELLBUTRIN	50MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	1985-12-30	`31067a03dcf5…`
2025-12-14 10:44 UTC · 2 captures of this ZIP	2025-12	N018644-002	WELLBUTRIN	75MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	1985-12-30	`31067a03dcf5…`
2025-12-14 10:44 UTC · 2 captures of this ZIP	2025-12	N018644-003	WELLBUTRIN	100MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	1985-12-30	`31067a03dcf5…`
2025-08-23 18:47 UTC	2025-08	N018644-001	WELLBUTRIN	50MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	1985-12-30	`6a471c1ec25d…`
2025-08-23 18:47 UTC	2025-08	N018644-002	WELLBUTRIN	75MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	1985-12-30	`6a471c1ec25d…`
2025-08-23 18:47 UTC	2025-08	N018644-003	WELLBUTRIN	100MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	1985-12-30	`6a471c1ec25d…`
2025-03-22 03:13 UTC · 3 captures of this ZIP	2025-03	N018644-001	WELLBUTRIN	50MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	1985-12-30	`fd3edfee7708…`
2025-03-22 03:13 UTC · 3 captures of this ZIP	2025-03	N018644-002	WELLBUTRIN	75MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	1985-12-30	`fd3edfee7708…`
2025-03-22 03:13 UTC · 3 captures of this ZIP	2025-03	N018644-003	WELLBUTRIN	100MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	1985-12-30	`fd3edfee7708…`
2025-02-26 10:13 UTC · 3 captures of this ZIP	2025-02	N018644-001	WELLBUTRIN	50MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	1985-12-30	`b8a1b40f171c…`
2025-02-26 10:13 UTC · 3 captures of this ZIP	2025-02	N018644-002	WELLBUTRIN	75MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	1985-12-30	`b8a1b40f171c…`
2025-02-26 10:13 UTC · 3 captures of this ZIP	2025-02	N018644-003	WELLBUTRIN	100MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	1985-12-30	`b8a1b40f171c…`
2025-01-19 17:59 UTC · 7 captures of this ZIP	2025-01	N018644-001	WELLBUTRIN	50MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	1985-12-30	`03ed91905a0d…`
2025-01-19 17:59 UTC · 7 captures of this ZIP	2025-01	N018644-002	WELLBUTRIN	75MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	1985-12-30	`03ed91905a0d…`
2025-01-19 17:59 UTC · 7 captures of this ZIP	2025-01	N018644-003	WELLBUTRIN	100MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	1985-12-30	`03ed91905a0d…`
2024-12-13 21:23 UTC · 2 captures of this ZIP	2024-12	N018644-001	WELLBUTRIN	50MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	1985-12-30	`2680178bc6a6…`
2024-12-13 21:23 UTC · 2 captures of this ZIP	2024-12	N018644-002	WELLBUTRIN	75MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	1985-12-30	`2680178bc6a6…`
2024-12-13 21:23 UTC · 2 captures of this ZIP	2024-12	N018644-003	WELLBUTRIN	100MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	1985-12-30	`2680178bc6a6…`
2024-09-14 05:58 UTC · 2 captures of this ZIP	2024-09	N018644-001	WELLBUTRIN	50MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	1985-12-30	`5bbf6a4d5a75…`
2024-09-14 05:58 UTC · 2 captures of this ZIP	2024-09	N018644-002	WELLBUTRIN	75MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	1985-12-30	`5bbf6a4d5a75…`
2024-09-14 05:58 UTC · 2 captures of this ZIP	2024-09	N018644-003	WELLBUTRIN	100MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	1985-12-30	`5bbf6a4d5a75…`
2024-11-08 22:44 UTC · 3 captures of this ZIP	2024-11	N018644-001	WELLBUTRIN	50MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	1985-12-30	`d8e5a09893c0…`
2024-11-08 22:44 UTC · 3 captures of this ZIP	2024-11	N018644-002	WELLBUTRIN	75MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	1985-12-30	`d8e5a09893c0…`
2024-11-08 22:44 UTC · 3 captures of this ZIP	2024-11	N018644-003	WELLBUTRIN	100MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	1985-12-30	`d8e5a09893c0…`
2024-10-29 15:01 UTC	2024-10	N018644-001	WELLBUTRIN	50MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	1985-12-30	`d06236e962d9…`
2024-10-29 15:01 UTC	2024-10	N018644-002	WELLBUTRIN	75MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	1985-12-30	`d06236e962d9…`
2024-10-29 15:01 UTC	2024-10	N018644-003	WELLBUTRIN	100MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	1985-12-30	`d06236e962d9…`
2024-08-13 05:28 UTC · 3 captures of this ZIP	2024-08	N018644-001	WELLBUTRIN	50MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	1985-12-30	`79d66fd596c7…`
2024-08-13 05:28 UTC · 3 captures of this ZIP	2024-08	N018644-002	WELLBUTRIN	75MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	1985-12-30	`79d66fd596c7…`
2024-08-13 05:28 UTC · 3 captures of this ZIP	2024-08	N018644-003	WELLBUTRIN	100MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	1985-12-30	`79d66fd596c7…`
2024-07-13 05:37 UTC · 2 captures of this ZIP	2024-07	N018644-001	WELLBUTRIN	50MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	1985-12-30	`301d65b070ca…`

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 9 of 12 · 236 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Bupropion Hydrochloride	BUPROPION HYDROCHLORIDE	Asclemed USA, Inc.	637e89e5-8f6e-4392-8045-a778cb9ed138	2025-02-12	Boxed warning, Warnings, Adverse reactions	Name fallback generic name: BUPROPION HYDROCHLORIDE
BUPROPION HYDROCHLORIDE	BUPROPION HYDROCHLORIDE	Preferred Pharmaceuticals Inc.	5dec4414-5595-46c9-ada9-3fbe98152040	2025-02-11	Boxed warning, Warnings, Adverse reactions	Name fallback generic name: BUPROPION HYDROCHLORIDE
Bupropion hydrochloride	BUPROPION HYDROCHLORIDE	Coupler LLC	2ccbf988-64b6-3a60-e063-6394a90ababa	2025-01-28	Boxed warning, Warnings, Adverse reactions	Name fallback generic name: BUPROPION HYDROCHLORIDE
Bupropion Hydrochloride	BUPROPION HYDROCHLORIDE	NuCare Pharmaceuticals,Inc.	d1043c87-0abe-ee8e-e053-2a95a90a419a	2025-01-23	Boxed warning, Warnings, Adverse reactions	Name fallback generic name: BUPROPION HYDROCHLORIDE
BUPROPION HYDROCHLORIDE	BUPROPION HYDROCHLORIDE	DIRECT RX	96d87edc-d12b-44b2-e053-2995a90a4e63	2025-01-22	Warnings, Adverse reactions	Name fallback generic name: BUPROPION HYDROCHLORIDE
Bupropion hydrochloride	BUPROPION HYDROCHLORIDE	Preferred Pharmaceuticals Inc.	1724f474-d6ab-46af-940f-7f874d4ff7fc	2025-01-21	Boxed warning, Warnings, Adverse reactions	Name fallback generic name: BUPROPION HYDROCHLORIDE
bupropion Hydrochloride	BUPROPION HYDROCHLORIDE	Bryant Ranch Prepack	4971c3cb-07c4-4c65-a16a-f1700e523147	2025-01-06	Boxed warning, Warnings, Adverse reactions	Name fallback generic name: BUPROPION HYDROCHLORIDE
bupropion Hydrochloride	BUPROPION HYDROCHLORIDE	Bryant Ranch Prepack	bd99969d-03d5-4609-88e8-a9ae93a83907	2025-01-06	Boxed warning, Warnings, Adverse reactions	Name fallback generic name: BUPROPION HYDROCHLORIDE
Bupropion Hydrochloride	BUPROPION HYDROCHLORIDE	NuCare Pharmaceuticals,Inc.	0e8b2109-8516-2d92-e063-6394a90a5d16	2025-01-03	Boxed warning, Warnings, Adverse reactions	Name fallback generic name: BUPROPION HYDROCHLORIDE
bupropion Hydrochloride	BUPROPION HYDROCHLORIDE	Aphena Pharma Solutions - Tennessee, LLC	d0eada89-e302-4ba3-bef0-e8c69af8206e	2025-01-02	Boxed warning, Warnings, Adverse reactions	Name fallback generic name: BUPROPION HYDROCHLORIDE
Bupropion Hydrochloride XL	BUPROPION HYDROCHLORIDE	Advanced Rx of Tennessee, LLC	2aabf040-16a6-b772-e063-6294a90afd70	2025-01-01	Boxed warning, Warnings, Adverse reactions	Name fallback generic name: BUPROPION HYDROCHLORIDE
Bupropion hydrochloride	BUPROPION HYDROCHLORIDE	Advanced Rx Pharmacy of Tennessee, LLC	f8af7829-8b61-6785-e053-6294a90af052	2024-12-31	Boxed warning, Warnings, Adverse reactions	Name fallback generic name: BUPROPION HYDROCHLORIDE
Bupropion Hydrochloride (XL)	BUPROPION HYDROCHLORIDE	Quality Care Products, LLC	57a9f4d3-0c41-4978-b81e-cf3059bc8c42	2024-12-19	Boxed warning, Warnings, Adverse reactions	Name fallback generic name: BUPROPION HYDROCHLORIDE
BUPROPION HYDROCHLORIDE	BUPROPION HYDROCHLORIDE	Advanced Rx of Tennessee, LLC	29a6c6e3-f30f-6541-e063-6394a90ae11d	2024-12-18	Boxed warning, Warnings, Adverse reactions	Name fallback generic name: BUPROPION HYDROCHLORIDE
Bupropion hydrochloride	BUPROPION HYDROCHLORIDE	Sun Pharmaceutical Industries, Inc.	29848192-7de3-4c0d-a822-1268dcf128b0	2024-12-09	Boxed warning, Warnings, Adverse reactions	Name fallback generic name: BUPROPION HYDROCHLORIDE
BUPROPION HYDROCHLORIDE	BUPROPION HYDROCHLORIDE	BluePoint Laboratories	5ccec958-998d-43a1-86fb-eb2b5e697b77	2024-11-30	Boxed warning, Warnings, Adverse reactions	Name fallback generic name: BUPROPION HYDROCHLORIDE
Bupropion hydrochloride	BUPROPION HYDROCHLORIDE	A-S Medication Solutions	bb63261f-ad18-4885-9ed7-e7dfde33e171	2024-10-31	Boxed warning, Warnings, Adverse reactions	Name fallback generic name: BUPROPION HYDROCHLORIDE
Bupropion hydrochloride	BUPROPION HYDROCHLORIDE	A-S Medication Solutions	a724b3b6-f60e-4b88-8603-8141a32075da	2024-10-31	Boxed warning, Warnings, Adverse reactions	Name fallback generic name: BUPROPION HYDROCHLORIDE
Bupropion Hydrochloride (XL)	BUPROPION HYDROCHLORIDE	A-S Medication Solutions	0ac739de-ad59-4882-810e-f52db22ac96f	2024-10-16	Boxed warning, Warnings, Adverse reactions	Name fallback generic name: BUPROPION HYDROCHLORIDE
Bupropion Hydrochloride (XL)	BUPROPION HYDROCHLORIDE	A-S Medication Solutions	d6efb695-c439-48d7-a155-5c661a5049af	2024-10-16	Boxed warning, Warnings, Adverse reactions	Name fallback generic name: BUPROPION HYDROCHLORIDE

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.

Documents#

Document, Submission type, Date table
Document	Submission type	Date
84107	SUPPL	2025-11-06
84106	SUPPL	2025-11-06
84078	SUPPL	2025-11-06
82435	SUPPL	2025-06-03
81111	SUPPL	2025-02-06
78429	SUPPL	2024-05-08
78418	SUPPL	2024-05-07
72827	SUPPL	2022-12-08
72826	SUPPL	2022-12-08
72818	SUPPL	2022-12-07
65004	SUPPL	2020-10-23
65003	SUPPL	2020-10-23
64971	SUPPL	2020-10-22
60829	SUPPL	2019-11-13
60828	SUPPL	2019-11-13
60800	SUPPL	2019-11-08
49479	SUPPL	2017-08-21
49456	SUPPL	2017-08-18
48359	SUPPL	2017-05-12
48354	SUPPL	2017-05-10
48303	SUPPL	2017-05-09
48263	SUPPL	2017-05-08
33536	SUPPL	2016-04-27
15066	SUPPL	2016-04-27
33534	SUPPL	2014-12-17
988	SUPPL	2014-12-17
33535	SUPPL	2014-07-22
15065	SUPPL	2014-07-21
20140	SUPPL	2014-07-07
20139	SUPPL	2014-07-07
15064	SUPPL	2013-12-26
987	SUPPL	2013-12-26
33533	SUPPL	2013-12-24
11257	SUPPL	2013-12-24
33532	SUPPL	2013-03-26
986	SUPPL	2013-03-21
15063	SUPPL	2012-08-03
40814	SUPPL	2012-06-26
15062	SUPPL	2011-07-28
11256	SUPPL	2011-07-25
33531	SUPPL	2011-05-23
15061	SUPPL	2011-05-19
11254	SUPPL	2010-05-28
15058	SUPPL	2010-05-27
15060	SUPPL	2010-03-03
15059	SUPPL	2009-07-07
985	SUPPL	2009-07-07
33530	SUPPL	2009-07-06
11255	SUPPL	2009-07-06
15057	SUPPL	2007-08-07
33529	SUPPL	2007-08-03
40813	SUPPL	2007-06-29
984	SUPPL	2007-02-02
983	SUPPL	2006-07-13
982	SUPPL	2006-07-13
33528	SUPPL	2006-07-05
11253	SUPPL	2006-07-05
15056	SUPPL	2006-03-03
44024	ORIG	2005-07-28
11252	SUPPL	2005-01-13
981	SUPPL	2005-01-13
980	SUPPL	2004-06-01
40812	SUPPL	2003-06-17
40811	SUPPL	2003-06-17
20138	SUPPL	2003-06-17
15055	SUPPL	2002-10-22
15053	SUPPL	2002-10-02
979	SUPPL	2002-10-02
15052	SUPPL	2002-06-20
15054	SUPPL	2002-02-12
57442	ORIG	1985-12-30