Application 020897

Type: NDA
Sponsor: JANSSEN PHARMS

Application Products#

Product, Drug, Ingredient table
Product	Drug	Ingredient	Form	Strength	Reference drug	Reference standard
001	DITROPAN XL	OXYBUTYNIN CHLORIDE	TABLET, EXTENDED RELEASE;ORAL	5MG	Yes	No
002	DITROPAN XL	OXYBUTYNIN CHLORIDE	TABLET, EXTENDED RELEASE;ORAL	10MG	Yes	No
003	DITROPAN XL	OXYBUTYNIN CHLORIDE	TABLET, EXTENDED RELEASE;ORAL	15MG Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons	Yes	No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
N020897-001	DITROPAN XL	OXYBUTYNIN CHLORIDE	5MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET, EXTENDED RELEASE / ORAL	RLD	1998-12-16
N020897-002	DITROPAN XL	OXYBUTYNIN CHLORIDE	10MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET, EXTENDED RELEASE / ORAL	RLD	1998-12-16
N020897-003	DITROPAN XL	OXYBUTYNIN CHLORIDE	15MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET, EXTENDED RELEASE / ORAL	RLD	1999-06-22

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	N020897-001	DITROPAN XL	5MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET, EXTENDED RELEASE / ORAL	RLD	1998-12-16	`84e616aacf4f…`
2026-09-14 22:38:34	2026-08	N020897-002	DITROPAN XL	10MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET, EXTENDED RELEASE / ORAL	RLD	1998-12-16	`84e616aacf4f…`
2026-09-14 22:38:34	2026-08	N020897-003	DITROPAN XL	15MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET, EXTENDED RELEASE / ORAL	RLD	1999-06-22	`84e616aacf4f…`
2026-08-18 06:07:40	2026-07	N020897-001	DITROPAN XL	5MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET, EXTENDED RELEASE / ORAL	RLD	1998-12-16	`caaa826d4ba7…`
2026-08-18 06:07:40	2026-07	N020897-002	DITROPAN XL	10MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET, EXTENDED RELEASE / ORAL	RLD	1998-12-16	`caaa826d4ba7…`
2026-08-18 06:07:40	2026-07	N020897-003	DITROPAN XL	15MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET, EXTENDED RELEASE / ORAL	RLD	1999-06-22	`caaa826d4ba7…`
2026-02-19 14:30 UTC	2026-02	N020897-001	DITROPAN XL	5MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET, EXTENDED RELEASE / ORAL	RLD	1998-12-16	`011fe1cb6892…`
2026-02-19 14:30 UTC	2026-02	N020897-002	DITROPAN XL	10MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET, EXTENDED RELEASE / ORAL	RLD	1998-12-16	`011fe1cb6892…`
2026-02-19 14:30 UTC	2026-02	N020897-003	DITROPAN XL	15MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET, EXTENDED RELEASE / ORAL	RLD	1999-06-22	`011fe1cb6892…`
2025-12-14 10:44 UTC · 2 captures of this ZIP	2025-12	N020897-001	DITROPAN XL	5MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET, EXTENDED RELEASE / ORAL	RLD	1998-12-16	`31067a03dcf5…`
2025-12-14 10:44 UTC · 2 captures of this ZIP	2025-12	N020897-002	DITROPAN XL	10MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET, EXTENDED RELEASE / ORAL	RLD	1998-12-16	`31067a03dcf5…`
2025-12-14 10:44 UTC · 2 captures of this ZIP	2025-12	N020897-003	DITROPAN XL	15MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET, EXTENDED RELEASE / ORAL	RLD	1999-06-22	`31067a03dcf5…`
2025-08-23 18:47 UTC	2025-08	N020897-001	DITROPAN XL	5MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET, EXTENDED RELEASE / ORAL	RLD	1998-12-16	`6a471c1ec25d…`
2025-08-23 18:47 UTC	2025-08	N020897-002	DITROPAN XL	10MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET, EXTENDED RELEASE / ORAL	RLD	1998-12-16	`6a471c1ec25d…`
2025-08-23 18:47 UTC	2025-08	N020897-003	DITROPAN XL	15MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET, EXTENDED RELEASE / ORAL	RLD	1999-06-22	`6a471c1ec25d…`
2025-03-22 03:13 UTC · 3 captures of this ZIP	2025-03	N020897-001	DITROPAN XL	5MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET, EXTENDED RELEASE / ORAL	RLD	1998-12-16	`fd3edfee7708…`
2025-03-22 03:13 UTC · 3 captures of this ZIP	2025-03	N020897-002	DITROPAN XL	10MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET, EXTENDED RELEASE / ORAL	RLD	1998-12-16	`fd3edfee7708…`
2025-03-22 03:13 UTC · 3 captures of this ZIP	2025-03	N020897-003	DITROPAN XL	15MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET, EXTENDED RELEASE / ORAL	RLD	1999-06-22	`fd3edfee7708…`
2025-02-26 10:13 UTC · 3 captures of this ZIP	2025-02	N020897-001	DITROPAN XL	5MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET, EXTENDED RELEASE / ORAL	RLD	1998-12-16	`b8a1b40f171c…`
2025-02-26 10:13 UTC · 3 captures of this ZIP	2025-02	N020897-002	DITROPAN XL	10MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET, EXTENDED RELEASE / ORAL	RLD	1998-12-16	`b8a1b40f171c…`
2025-02-26 10:13 UTC · 3 captures of this ZIP	2025-02	N020897-003	DITROPAN XL	15MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET, EXTENDED RELEASE / ORAL	RLD	1999-06-22	`b8a1b40f171c…`
2025-01-19 17:59 UTC · 7 captures of this ZIP	2025-01	N020897-001	DITROPAN XL	5MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET, EXTENDED RELEASE / ORAL	RLD	1998-12-16	`03ed91905a0d…`
2025-01-19 17:59 UTC · 7 captures of this ZIP	2025-01	N020897-002	DITROPAN XL	10MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET, EXTENDED RELEASE / ORAL	RLD	1998-12-16	`03ed91905a0d…`
2025-01-19 17:59 UTC · 7 captures of this ZIP	2025-01	N020897-003	DITROPAN XL	15MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET, EXTENDED RELEASE / ORAL	RLD	1999-06-22	`03ed91905a0d…`
2024-12-13 21:23 UTC · 2 captures of this ZIP	2024-12	N020897-001	DITROPAN XL	5MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET, EXTENDED RELEASE / ORAL	RLD	1998-12-16	`2680178bc6a6…`
2024-12-13 21:23 UTC · 2 captures of this ZIP	2024-12	N020897-002	DITROPAN XL	10MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET, EXTENDED RELEASE / ORAL	RLD	1998-12-16	`2680178bc6a6…`
2024-12-13 21:23 UTC · 2 captures of this ZIP	2024-12	N020897-003	DITROPAN XL	15MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET, EXTENDED RELEASE / ORAL	RLD	1999-06-22	`2680178bc6a6…`
2024-09-14 05:58 UTC · 2 captures of this ZIP	2024-09	N020897-001	DITROPAN XL	5MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET, EXTENDED RELEASE / ORAL	RLD	1998-12-16	`5bbf6a4d5a75…`
2024-09-14 05:58 UTC · 2 captures of this ZIP	2024-09	N020897-002	DITROPAN XL	10MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET, EXTENDED RELEASE / ORAL	RLD	1998-12-16	`5bbf6a4d5a75…`
2024-09-14 05:58 UTC · 2 captures of this ZIP	2024-09	N020897-003	DITROPAN XL	15MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET, EXTENDED RELEASE / ORAL	RLD	1999-06-22	`5bbf6a4d5a75…`
2024-11-08 22:44 UTC · 3 captures of this ZIP	2024-11	N020897-001	DITROPAN XL	5MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET, EXTENDED RELEASE / ORAL	RLD	1998-12-16	`d8e5a09893c0…`
2024-11-08 22:44 UTC · 3 captures of this ZIP	2024-11	N020897-002	DITROPAN XL	10MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET, EXTENDED RELEASE / ORAL	RLD	1998-12-16	`d8e5a09893c0…`
2024-11-08 22:44 UTC · 3 captures of this ZIP	2024-11	N020897-003	DITROPAN XL	15MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET, EXTENDED RELEASE / ORAL	RLD	1999-06-22	`d8e5a09893c0…`
2024-10-29 15:01 UTC	2024-10	N020897-001	DITROPAN XL	5MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET, EXTENDED RELEASE / ORAL	RLD	1998-12-16	`d06236e962d9…`
2024-10-29 15:01 UTC	2024-10	N020897-002	DITROPAN XL	10MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET, EXTENDED RELEASE / ORAL	RLD	1998-12-16	`d06236e962d9…`
2024-10-29 15:01 UTC	2024-10	N020897-003	DITROPAN XL	15MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET, EXTENDED RELEASE / ORAL	RLD	1999-06-22	`d06236e962d9…`
2024-08-13 05:28 UTC · 3 captures of this ZIP	2024-08	N020897-001	DITROPAN XL	5MG	TABLET, EXTENDED RELEASE / ORAL	RLD	1998-12-16	`79d66fd596c7…`
2024-08-13 05:28 UTC · 3 captures of this ZIP	2024-08	N020897-002	DITROPAN XL	10MG	TABLET, EXTENDED RELEASE / ORAL	RLD	1998-12-16	`79d66fd596c7…`
2024-08-13 05:28 UTC · 3 captures of this ZIP	2024-08	N020897-003	DITROPAN XL	15MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET, EXTENDED RELEASE / ORAL	RLD	1999-06-22	`79d66fd596c7…`
2024-07-13 05:37 UTC · 2 captures of this ZIP	2024-07	N020897-001	DITROPAN XL	5MG	TABLET, EXTENDED RELEASE / ORAL	RLD	1998-12-16	`301d65b070ca…`

Observed Orange Book normalized TE history#

Normalized TE history page 1 of 2 · 42 observed states.

Captured, Edition, Application-product table
Captured	Edition	Application-product	TE code	Order	Source SHA-256
2022-06-29 02:47 UTC · 2 captures of this ZIP	2022-06	N020897-001	AB	1	`5c6f7cd8ea54…`
2022-06-29 02:47 UTC · 2 captures of this ZIP	2022-06	N020897-002	AB	1	`5c6f7cd8ea54…`
2022-04-08 23:34 UTC	2022-04	N020897-001	AB	1	`5d02ea3f76ae…`
2022-04-08 23:34 UTC	2022-04	N020897-002	AB	1	`5d02ea3f76ae…`
2022-04-04 05:41 UTC	2022-04	N020897-001	AB	1	`4b0b4de00fa7…`
2022-04-04 05:41 UTC	2022-04	N020897-002	AB	1	`4b0b4de00fa7…`
2019-12-13 00:20 UTC	2019-12	N020897-001	AB	1	`74a2ff9319b5…`
2019-12-13 00:20 UTC	2019-12	N020897-002	AB	1	`74a2ff9319b5…`
2022-03-09 01:35 UTC	2022-03	N020897-001	AB	1	`bb7c543d1eb4…`
2022-03-09 01:35 UTC	2022-03	N020897-002	AB	1	`bb7c543d1eb4…`
2021-12-28 21:50 UTC	2021-12	N020897-001	AB	1	`782e0a99824c…`
2021-12-28 21:50 UTC	2021-12	N020897-002	AB	1	`782e0a99824c…`
2021-05-05 16:15 UTC · 3 captures of this ZIP	2021-05	N020897-001	AB	1	`87673890dc5c…`
2021-05-05 16:15 UTC · 3 captures of this ZIP	2021-05	N020897-002	AB	1	`87673890dc5c…`
2021-03-12 10:30 UTC	2021-03	N020897-001	AB	1	`5aa47cf7b7d7…`
2021-03-12 10:30 UTC	2021-03	N020897-002	AB	1	`5aa47cf7b7d7…`
2020-12-22 03:56 UTC	2020-12	N020897-001	AB	1	`8869cabd3fbd…`
2020-12-22 03:56 UTC	2020-12	N020897-002	AB	1	`8869cabd3fbd…`
2020-11-12 02:37 UTC	2020-11	N020897-001	AB	1	`c0c555d07b60…`
2020-11-12 02:37 UTC	2020-11	N020897-002	AB	1	`c0c555d07b60…`
2019-12-14 00:12 UTC	2019-12	N020897-001	AB	1	`3f01610625f2…`
2019-12-14 00:12 UTC	2019-12	N020897-002	AB	1	`3f01610625f2…`
2019-09-15 20:21 UTC	2019-09	N020897-001	AB	1	`b00525d2431f…`
2019-09-15 20:21 UTC	2019-09	N020897-002	AB	1	`b00525d2431f…`
2019-07-19 19:46 UTC	2019-07	N020897-001	AB	1	`ea99ee380514…`
2019-07-19 19:46 UTC	2019-07	N020897-002	AB	1	`ea99ee380514…`
2023-07-15 15:27 UTC · 2 captures of this ZIP	2023-07	N020897-001	AB	1	`a67488948f0b…`
2023-07-15 15:27 UTC · 2 captures of this ZIP	2023-07	N020897-002	AB	1	`a67488948f0b…`
2023-06-13 01:57 UTC · 3 captures of this ZIP	2023-06	N020897-001	AB	1	`3f0d92c62455…`
2023-06-13 01:57 UTC · 3 captures of this ZIP	2023-06	N020897-002	AB	1	`3f0d92c62455…`
2023-05-13 08:27 UTC	2023-05	N020897-001	AB	1	`053a50430f4f…`
2023-05-13 08:27 UTC	2023-05	N020897-002	AB	1	`053a50430f4f…`
2023-01-26 05:58 UTC	2023-01	N020897-001	AB	1	`3bdfa0b2c4d7…`
2023-01-26 05:58 UTC	2023-01	N020897-002	AB	1	`3bdfa0b2c4d7…`
2022-11-12 20:34 UTC · 5 captures of this ZIP	2022-11	N020897-001	AB	1	`3a93d1ddd44b…`
2022-11-12 20:34 UTC · 5 captures of this ZIP	2022-11	N020897-002	AB	1	`3a93d1ddd44b…`
2022-10-28 04:53 UTC	2022-10	N020897-001	AB	1	`f41ea6bd6efb…`
2022-10-28 04:53 UTC	2022-10	N020897-002	AB	1	`f41ea6bd6efb…`
2022-09-29 23:25 UTC	2022-09	N020897-001	AB	1	`e64feba35796…`
2022-09-29 23:25 UTC	2022-09	N020897-002	AB	1	`e64feba35796…`

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 4 of 4 · 77 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Oxybutynin Chloride Extended Release	OXYBUTYNIN CHLORIDE	Proficient Rx LP	7d2332b4-9e48-4bb2-a2c3-75e16e1d455b	2024-04-01	Warnings, Adverse reactions	Name fallback generic name: OXYBUTYNIN CHLORIDE
Oxybutynin Chloride Extended Release	OXYBUTYNIN CHLORIDE	Bryant Ranch Prepack	2f898b29-46cf-4427-bb64-8c30532222f5	2024-01-18	Warnings, Adverse reactions	Name fallback generic name: OXYBUTYNIN CHLORIDE
Oxybutynin Chloride	OXYBUTYNIN CHLORIDE	A-S Medication Solutions	5e3b454b-6d3c-418b-8ac2-b0e17f018bbf	2023-12-27	Warnings, Adverse reactions	Name fallback generic name: OXYBUTYNIN CHLORIDE
Oxybutynin Chloride	OXYBUTYNIN CHLORIDE	A-S Medication Solutions	afc6a3aa-e43d-4f10-bdbd-570a149bf9db	2023-12-27	Warnings, Adverse reactions	Name fallback generic name: OXYBUTYNIN CHLORIDE
OXYBUTYNIN CHLORIDE	OXYBUTYNIN CHLORIDE	A-S Medication Solutions	83522acd-0ecc-46ac-a018-a3205ba096ff	2023-11-01	Warnings, Adverse reactions	Name fallback generic name: OXYBUTYNIN CHLORIDE
OXYBUTYNIN CHLORIDE	OXYBUTYNIN CHLORIDE	NCS HealthCare of KY, LLC dba Vangard Labs	5b72d34e-ae57-4459-ba2c-3bae8a69c5c1	2023-10-04	Warnings, Adverse reactions	Name fallback generic name: OXYBUTYNIN CHLORIDE
Oxybutynin Chloride Extended Release	OXYBUTYNIN CHLORIDE	Aphena Pharma Solutions - Tennessee, LLC	02ff3be7-fc5c-4b91-8c67-ecdf6e19c42a	2023-05-31	Warnings, Adverse reactions	Name fallback generic name: OXYBUTYNIN CHLORIDE
Oxybutynin Chloride	OXYBUTYNIN CHLORIDE	Aphena Pharma Solutions - Tennessee, LLC	d2bb6927-5fbf-49ca-a891-d701bff1c812	2023-05-31	Warnings, Adverse reactions	Name fallback generic name: OXYBUTYNIN CHLORIDE
Oxybutynin Chloride Extended Release	OXYBUTYNIN CHLORIDE	Lannett Company, Inc.	c5950dba-d92b-46a0-993f-af9f9ddb52bf	2023-05-30	Warnings, Adverse reactions	Name fallback generic name: OXYBUTYNIN CHLORIDE
Oxybutynin Chloride	OXYBUTYNIN CHLORIDE	Amneal Pharmaceuticals LLC	53924eba-1919-4203-9a1e-d57dfdd3b963	2023-02-02	Warnings, Adverse reactions	Name fallback generic name: OXYBUTYNIN CHLORIDE
Oxybutynin Chloride	OXYBUTYNIN CHLORIDE	Aphena Pharma Solutions - Tennessee, LLC	1e1c1043-e4c5-4a06-9cc1-45d4397746f4	2023-01-04	Warnings, Adverse reactions	Name fallback generic name: OXYBUTYNIN CHLORIDE
Oxybutynin Chloride	OXYBUTYNIN CHLORIDE	Proficient Rx LP	e3f0c249-8085-4979-823a-820e233a284f	2022-06-01	Warnings, Adverse reactions	Name fallback generic name: OXYBUTYNIN CHLORIDE
oxybutynin chloride	OXYBUTYNIN CHLORIDE	Proficient Rx LP	88f08450-559e-4038-aad1-051e4ab283cf	2022-06-01	Warnings, Adverse reactions	Name fallback generic name: OXYBUTYNIN CHLORIDE
OXYBUTYNIN CHLORIDE	OXYBUTYNIN CHLORIDE	Leading Pharma, LLC	b73b8338-8045-448f-87a6-3d289227d00e	2022-02-14	Warnings, Adverse reactions	Name fallback generic name: OXYBUTYNIN CHLORIDE
Oxybutynin Chloride	OXYBUTYNIN CHLORIDE	Lannett Company, Inc.	615f3d95-197c-4fec-b81f-c26449c93c3b	2020-02-21	Warnings, Adverse reactions	Name fallback generic name: OXYBUTYNIN CHLORIDE
Oxybutynin Chloride Extended Release	OXYBUTYNIN CHLORIDE	Aphena Pharma Solutions - Tennessee, LLC	e985e201-2fb3-4781-9790-a1a3db1ae2a1	2017-10-20	Warnings, Adverse reactions	Name fallback generic name: OXYBUTYNIN CHLORIDE
Oxybutynin Chloride	OXYBUTYNIN CHLORIDE	Aphena Pharma Solutions - Tennessee, LLC	58136f28-70c1-4cf2-bcd7-858c5609431a	2016-06-15	Warnings, Adverse reactions	Name fallback generic name: OXYBUTYNIN CHLORIDE

Reported adverse events (FAERS/openFDA)#

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

NDC Listings For This Application#

NDC listings for this application page 1 of 1 · 21 matching rows.

NDC, Name, Nonproprietary name table
NDC	Name	Nonproprietary name	Labeler	Marketing category	Status
0615-7521	oxybutynin chloride	oxybutynin chloride	NCS HealthCare of KY, Inc dba Vangard Labs	NDA	Current
10147-0761	Oxybutynin Chloride	oxybutynin chloride	Patriot Pharmaceuticals, LLC	NDA	Current
10147-0761	Oxybutynin Chloride	oxybutynin chloride	Patriot Pharmaceuticals,	NDA	Current
10147-0761	Oxybutynin Chloride	oxybutynin chloride	Patriot Pharmaceuticals, LLC	NDA	Current
10147-0771	Oxybutynin Chloride	oxybutynin chloride	Patriot Pharmaceuticals, LLC	NDA	Current
10147-0771	Oxybutynin Chloride	oxybutynin chloride	Patriot Pharmaceuticals,	NDA	Current
10147-0771	Oxybutynin Chloride	oxybutynin chloride	Patriot Pharmaceuticals, LLC	NDA	Current
50458-805	Ditropan	oxybutynin chloride	Janssen Pharmaceuticals, Inc.	NDA	Current
50458-805	Ditropan	oxybutynin chloride	Janssen Pharmaceuticals, Inc.	NDA	Current
50458-805	Ditropan	oxybutynin chloride	Janssen Pharmaceuticals, Inc.	NDA	Current
50458-805	Ditropan	oxybutynin chloride	Janssen Pharmaceuticals, Inc.	NDA	Current
50458-805	Ditropan	oxybutynin chloride	Janssen Pharmaceuticals, Inc.	NDA	Current
50458-805	Ditropan	oxybutynin chloride	Janssen Pharmaceuticals, Inc.	NDA	Current
50458-805	Ditropan	oxybutynin chloride	Janssen Pharmaceuticals, Inc.	NDA	Current
50458-810	Ditropan	oxybutynin chloride	Janssen Pharmaceuticals, Inc.	NDA	Current
50458-810	Ditropan	oxybutynin chloride	Janssen Pharmaceuticals, Inc.	NDA	Current
50458-810	Ditropan	oxybutynin chloride	Janssen Pharmaceuticals, Inc.	NDA	Current
50458-810	Ditropan	oxybutynin chloride	Janssen Pharmaceuticals, Inc.	NDA	Current
50458-810	Ditropan	oxybutynin chloride	Janssen Pharmaceuticals, Inc.	NDA	Current
50458-810	Ditropan	oxybutynin chloride	Janssen Pharmaceuticals, Inc.	NDA	Current
50458-810	Ditropan	oxybutynin chloride	Janssen Pharmaceuticals, Inc.	NDA	Current

Documents#

Document, Submission type, Date table
Document	Submission type	Date
66923	SUPPL	2021-03-30
66920	SUPPL	2021-03-30
59998	SUPPL	2019-09-13
59997	SUPPL	2019-09-13
56191	SUPPL	2018-11-06
56138	SUPPL	2018-10-29
45407	SUPPL	2016-09-28
45294	SUPPL	2016-09-15
35595	SUPPL	2015-03-04
3684	SUPPL	2015-03-02
35594	SUPPL	2013-08-09
26140	SUPPL	2013-08-05
13693	SUPPL	2012-11-15
26139	SUPPL	2012-11-14
35593	SUPPL	2012-03-27
3683	SUPPL	2012-03-27
35592	SUPPL	2011-12-20
26138	SUPPL	2011-12-20
3682	SUPPL	2011-07-05
13692	SUPPL	2011-06-30
13691	SUPPL	2009-07-23
26137	SUPPL	2009-07-17
3681	SUPPL	2008-03-17
13690	SUPPL	2008-02-14
41790	SUPPL	2007-04-11
35591	SUPPL	2004-07-01
26136	SUPPL	2004-06-30
3680	SUPPL	2003-05-29
35590	SUPPL	2003-04-16
13689	SUPPL	2003-04-16
35589	ORIG	1998-12-16
26135	ORIG	1998-12-16
21049	ORIG	1998-12-16
53120	ORIG	1900-01-01
53119	ORIG	1900-01-01
53118	ORIG	1900-01-01