REQUIP

Product NDC: 0007-4896
11-digit product format: 000074896
Labeler code: 0007
Product ID: 0007-4896_1f8d4972-d7e0-4f31-a10c-6ff0936047b1
Type: HUMAN PRESCRIPTION DRUG
Nonproprietary name: ropinirole
Dosage form: TABLET, FILM COATED
Route: ORAL
Labeler: GlaxoSmithKline LLC
Application: NDA020658
Marketing category: NDA
Marketing start: 1999-09-21
Marketing end: 2019-11-30
Substance: ROPINIROLE HYDROCHLORIDE
Active strength: 4 mg/1
Pharmacologic classes: Dopamine Agonists [MoA],Nonergot Dopamine Agonist [EPC]
NDC exclude flag: No
Listing certified through: 0000-00-00
Current FDA listing: Historical FDA.report record

NDC auxiliary status#

These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.

Current NDC status page 1 of 1 · 2 matching rows.

Dataset, Scope, Product NDC table
Dataset	Scope	Product NDC	Package NDC	Code	Status	Reporting period	Source date
excluded product	product	0007-4896		D	Discontinued by firm		2026-08-10
excluded package	package	0007-4896	0007-4896-20	D	Discontinued by firm		2026-08-10

Observed NDC auxiliary status history#

This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.

Historic NDC status page 1 of 1 · 24 matching rows.

View current auxiliary records. · View the auxiliary file history.

Captured / source date, Dataset, Scope table
Captured / source date	Dataset	Scope	Package NDC	Snapshot	Source SHA-256
2025-12-14 17:58 UTC · source 2025-12-05	excluded product	product		`d630ba8d3edf…`	`732f749b63fb…`
2025-12-14 17:58 UTC · source 2025-12-05	excluded package	package	0007-4896-20	`d630ba8d3edf…`	`732f749b63fb…`
2025-08-27 00:01 UTC · source 2025-08-26	excluded product	product		`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-08-27 00:01 UTC · source 2025-08-26	excluded package	package	0007-4896-20	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-04-01 02:39 UTC · source 2025-03-31	excluded product	product		`2ef7874e63bc…`	`57b86245f4fa…`
2025-04-01 02:39 UTC · source 2025-03-31	excluded package	package	0007-4896-20	`2ef7874e63bc…`	`57b86245f4fa…`
2025-03-28 20:22 UTC · source 2025-03-28	excluded product	product		`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-28 20:22 UTC · source 2025-03-28	excluded package	package	0007-4896-20	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-22 03:12 UTC · source 2025-03-21	excluded product	product		`cfe11265f3b6…`	`090c488252e2…`
2025-03-22 03:12 UTC · source 2025-03-21	excluded package	package	0007-4896-20	`cfe11265f3b6…`	`090c488252e2…`
2025-03-10 12:48 UTC · source 2025-03-10	excluded product	product		`cdf11ea48f46…`	`ba0047e9e063…`
2025-03-10 12:48 UTC · source 2025-03-10	excluded package	package	0007-4896-20	`cdf11ea48f46…`	`ba0047e9e063…`
2025-02-02 03:52 UTC · source 2025-01-31	excluded product	product		`302b2466d912…`	`e7b80fea0513…`
2025-02-02 03:52 UTC · source 2025-01-31	excluded package	package	0007-4896-20	`302b2466d912…`	`e7b80fea0513…`
2025-01-20 13:05 UTC · source 2025-01-20	excluded product	product		`ed331223b511…`	`672a5bd82f5f…`
2025-01-20 13:05 UTC · source 2025-01-20	excluded package	package	0007-4896-20	`ed331223b511…`	`672a5bd82f5f…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded product	product		`0efc9e666f02…`	`f202fb6c5f17…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded package	package	0007-4896-20	`0efc9e666f02…`	`f202fb6c5f17…`
2024-11-09 02:27 UTC · source 2024-11-08	excluded product	product		`ad56d346431e…`	`cc804d4bbf1e…`
2024-11-09 02:27 UTC · source 2024-11-08	excluded package	package	0007-4896-20	`ad56d346431e…`	`cc804d4bbf1e…`
2024-10-04 04:10 UTC · source 2024-10-03	excluded product	product		`367a005e9d99…`	`383a685ebd0f…`
2024-10-04 04:10 UTC · source 2024-10-03	excluded package	package	0007-4896-20	`367a005e9d99…`	`383a685ebd0f…`
2024-07-10 04:00 UTC · source 2024-07-09	excluded product	product		`557ba5c1ecfa…`	`9c80585c8c6e…`
2024-07-10 04:00 UTC · source 2024-07-09	excluded package	package	0007-4896-20	`557ba5c1ecfa…`	`9c80585c8c6e…`

Source provenance: Browse the complete Orange Book source catalog · source snapshot 1.

Orange Book products#

Current product rows page 1 of 1 · 7 matching rows.

Application-product, Trade name, Ingredient table
Application-product	Trade name	Ingredient	Strength	Dosage form / route	RLD / RS	Approval date
N020658-001	REQUIP	ROPINIROLE HYDROCHLORIDE	EQ 0.25MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	1997-09-19
N020658-002	REQUIP	ROPINIROLE HYDROCHLORIDE	EQ 0.5MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	1997-09-19
N020658-003	REQUIP	ROPINIROLE HYDROCHLORIDE	EQ 1MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	1997-09-19
N020658-004	REQUIP	ROPINIROLE HYDROCHLORIDE	EQ 2MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	1997-09-19
N020658-005	REQUIP	ROPINIROLE HYDROCHLORIDE	EQ 5MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	1997-09-19
N020658-006	REQUIP	ROPINIROLE HYDROCHLORIDE	EQ 3MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	1999-01-27
N020658-007	REQUIP	ROPINIROLE HYDROCHLORIDE	EQ 4MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	1999-01-27

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 8 · 287 observed states.

Captured, Edition, Application-product table
Captured	Edition	Application-product	Trade name	Strength	Dosage form / route	RLD / RS	Approval date	Source SHA-256
2026-02-19 14:30 UTC	2026-02	N020658-001	REQUIP	EQ 0.25MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	1997-09-19	`011fe1cb6892…`
2026-02-19 14:30 UTC	2026-02	N020658-002	REQUIP	EQ 0.5MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	1997-09-19	`011fe1cb6892…`
2026-02-19 14:30 UTC	2026-02	N020658-003	REQUIP	EQ 1MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	1997-09-19	`011fe1cb6892…`
2026-02-19 14:30 UTC	2026-02	N020658-004	REQUIP	EQ 2MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	1997-09-19	`011fe1cb6892…`
2026-02-19 14:30 UTC	2026-02	N020658-005	REQUIP	EQ 5MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	1997-09-19	`011fe1cb6892…`
2026-02-19 14:30 UTC	2026-02	N020658-006	REQUIP	EQ 3MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	1999-01-27	`011fe1cb6892…`
2026-02-19 14:30 UTC	2026-02	N020658-007	REQUIP	EQ 4MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	1999-01-27	`011fe1cb6892…`
2025-12-14 10:44 UTC · 2 captures of this ZIP	2025-12	N020658-001	REQUIP	EQ 0.25MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	1997-09-19	`31067a03dcf5…`
2025-12-14 10:44 UTC · 2 captures of this ZIP	2025-12	N020658-002	REQUIP	EQ 0.5MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	1997-09-19	`31067a03dcf5…`
2025-12-14 10:44 UTC · 2 captures of this ZIP	2025-12	N020658-003	REQUIP	EQ 1MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	1997-09-19	`31067a03dcf5…`
2025-12-14 10:44 UTC · 2 captures of this ZIP	2025-12	N020658-004	REQUIP	EQ 2MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	1997-09-19	`31067a03dcf5…`
2025-12-14 10:44 UTC · 2 captures of this ZIP	2025-12	N020658-005	REQUIP	EQ 5MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	1997-09-19	`31067a03dcf5…`
2025-12-14 10:44 UTC · 2 captures of this ZIP	2025-12	N020658-006	REQUIP	EQ 3MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	1999-01-27	`31067a03dcf5…`
2025-12-14 10:44 UTC · 2 captures of this ZIP	2025-12	N020658-007	REQUIP	EQ 4MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	1999-01-27	`31067a03dcf5…`
2025-08-23 18:47 UTC	2025-08	N020658-001	REQUIP	EQ 0.25MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	1997-09-19	`6a471c1ec25d…`
2025-08-23 18:47 UTC	2025-08	N020658-002	REQUIP	EQ 0.5MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	1997-09-19	`6a471c1ec25d…`
2025-08-23 18:47 UTC	2025-08	N020658-003	REQUIP	EQ 1MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	1997-09-19	`6a471c1ec25d…`
2025-08-23 18:47 UTC	2025-08	N020658-004	REQUIP	EQ 2MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	1997-09-19	`6a471c1ec25d…`
2025-08-23 18:47 UTC	2025-08	N020658-005	REQUIP	EQ 5MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	1997-09-19	`6a471c1ec25d…`
2025-08-23 18:47 UTC	2025-08	N020658-006	REQUIP	EQ 3MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	1999-01-27	`6a471c1ec25d…`
2025-08-23 18:47 UTC	2025-08	N020658-007	REQUIP	EQ 4MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	1999-01-27	`6a471c1ec25d…`
2025-03-22 03:13 UTC · 3 captures of this ZIP	2025-03	N020658-001	REQUIP	EQ 0.25MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	1997-09-19	`fd3edfee7708…`
2025-03-22 03:13 UTC · 3 captures of this ZIP	2025-03	N020658-002	REQUIP	EQ 0.5MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	1997-09-19	`fd3edfee7708…`
2025-03-22 03:13 UTC · 3 captures of this ZIP	2025-03	N020658-003	REQUIP	EQ 1MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	1997-09-19	`fd3edfee7708…`
2025-03-22 03:13 UTC · 3 captures of this ZIP	2025-03	N020658-004	REQUIP	EQ 2MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	1997-09-19	`fd3edfee7708…`
2025-03-22 03:13 UTC · 3 captures of this ZIP	2025-03	N020658-005	REQUIP	EQ 5MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	1997-09-19	`fd3edfee7708…`
2025-03-22 03:13 UTC · 3 captures of this ZIP	2025-03	N020658-006	REQUIP	EQ 3MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	1999-01-27	`fd3edfee7708…`
2025-03-22 03:13 UTC · 3 captures of this ZIP	2025-03	N020658-007	REQUIP	EQ 4MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	1999-01-27	`fd3edfee7708…`
2025-02-26 10:13 UTC · 3 captures of this ZIP	2025-02	N020658-001	REQUIP	EQ 0.25MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	1997-09-19	`b8a1b40f171c…`
2025-02-26 10:13 UTC · 3 captures of this ZIP	2025-02	N020658-002	REQUIP	EQ 0.5MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	1997-09-19	`b8a1b40f171c…`
2025-02-26 10:13 UTC · 3 captures of this ZIP	2025-02	N020658-003	REQUIP	EQ 1MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	1997-09-19	`b8a1b40f171c…`
2025-02-26 10:13 UTC · 3 captures of this ZIP	2025-02	N020658-004	REQUIP	EQ 2MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	1997-09-19	`b8a1b40f171c…`
2025-02-26 10:13 UTC · 3 captures of this ZIP	2025-02	N020658-005	REQUIP	EQ 5MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	1997-09-19	`b8a1b40f171c…`
2025-02-26 10:13 UTC · 3 captures of this ZIP	2025-02	N020658-006	REQUIP	EQ 3MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	1999-01-27	`b8a1b40f171c…`
2025-02-26 10:13 UTC · 3 captures of this ZIP	2025-02	N020658-007	REQUIP	EQ 4MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	1999-01-27	`b8a1b40f171c…`
2025-01-19 17:59 UTC · 7 captures of this ZIP	2025-01	N020658-001	REQUIP	EQ 0.25MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	1997-09-19	`03ed91905a0d…`
2025-01-19 17:59 UTC · 7 captures of this ZIP	2025-01	N020658-002	REQUIP	EQ 0.5MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	1997-09-19	`03ed91905a0d…`
2025-01-19 17:59 UTC · 7 captures of this ZIP	2025-01	N020658-003	REQUIP	EQ 1MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	1997-09-19	`03ed91905a0d…`
2025-01-19 17:59 UTC · 7 captures of this ZIP	2025-01	N020658-004	REQUIP	EQ 2MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	1997-09-19	`03ed91905a0d…`
2025-01-19 17:59 UTC · 7 captures of this ZIP	2025-01	N020658-005	REQUIP	EQ 5MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	1997-09-19	`03ed91905a0d…`

Observed Orange Book normalized TE history#

Normalized TE history page 1 of 2 · 56 observed states.

Captured, Edition, Application-product table
Captured	Edition	Application-product	TE code	Order	Source SHA-256
2019-12-13 00:20 UTC	2019-12	N020658-001	AB	1	`74a2ff9319b5…`
2019-12-13 00:20 UTC	2019-12	N020658-002	AB	1	`74a2ff9319b5…`
2019-12-13 00:20 UTC	2019-12	N020658-003	AB	1	`74a2ff9319b5…`
2019-12-13 00:20 UTC	2019-12	N020658-004	AB	1	`74a2ff9319b5…`
2019-12-13 00:20 UTC	2019-12	N020658-005	AB	1	`74a2ff9319b5…`
2019-12-13 00:20 UTC	2019-12	N020658-006	AB	1	`74a2ff9319b5…`
2019-12-13 00:20 UTC	2019-12	N020658-007	AB	1	`74a2ff9319b5…`
2021-05-05 16:15 UTC · 3 captures of this ZIP	2021-05	N020658-001	AB	1	`87673890dc5c…`
2021-05-05 16:15 UTC · 3 captures of this ZIP	2021-05	N020658-002	AB	1	`87673890dc5c…`
2021-05-05 16:15 UTC · 3 captures of this ZIP	2021-05	N020658-003	AB	1	`87673890dc5c…`
2021-05-05 16:15 UTC · 3 captures of this ZIP	2021-05	N020658-004	AB	1	`87673890dc5c…`
2021-05-05 16:15 UTC · 3 captures of this ZIP	2021-05	N020658-005	AB	1	`87673890dc5c…`
2021-05-05 16:15 UTC · 3 captures of this ZIP	2021-05	N020658-006	AB	1	`87673890dc5c…`
2021-05-05 16:15 UTC · 3 captures of this ZIP	2021-05	N020658-007	AB	1	`87673890dc5c…`
2021-03-12 10:30 UTC	2021-03	N020658-001	AB	1	`5aa47cf7b7d7…`
2021-03-12 10:30 UTC	2021-03	N020658-002	AB	1	`5aa47cf7b7d7…`
2021-03-12 10:30 UTC	2021-03	N020658-003	AB	1	`5aa47cf7b7d7…`
2021-03-12 10:30 UTC	2021-03	N020658-004	AB	1	`5aa47cf7b7d7…`
2021-03-12 10:30 UTC	2021-03	N020658-005	AB	1	`5aa47cf7b7d7…`
2021-03-12 10:30 UTC	2021-03	N020658-006	AB	1	`5aa47cf7b7d7…`
2021-03-12 10:30 UTC	2021-03	N020658-007	AB	1	`5aa47cf7b7d7…`
2020-12-22 03:56 UTC	2020-12	N020658-001	AB	1	`8869cabd3fbd…`
2020-12-22 03:56 UTC	2020-12	N020658-002	AB	1	`8869cabd3fbd…`
2020-12-22 03:56 UTC	2020-12	N020658-003	AB	1	`8869cabd3fbd…`
2020-12-22 03:56 UTC	2020-12	N020658-004	AB	1	`8869cabd3fbd…`
2020-12-22 03:56 UTC	2020-12	N020658-005	AB	1	`8869cabd3fbd…`
2020-12-22 03:56 UTC	2020-12	N020658-006	AB	1	`8869cabd3fbd…`
2020-12-22 03:56 UTC	2020-12	N020658-007	AB	1	`8869cabd3fbd…`
2020-11-12 02:37 UTC	2020-11	N020658-001	AB	1	`c0c555d07b60…`
2020-11-12 02:37 UTC	2020-11	N020658-002	AB	1	`c0c555d07b60…`
2020-11-12 02:37 UTC	2020-11	N020658-003	AB	1	`c0c555d07b60…`
2020-11-12 02:37 UTC	2020-11	N020658-004	AB	1	`c0c555d07b60…`
2020-11-12 02:37 UTC	2020-11	N020658-005	AB	1	`c0c555d07b60…`
2020-11-12 02:37 UTC	2020-11	N020658-006	AB	1	`c0c555d07b60…`
2020-11-12 02:37 UTC	2020-11	N020658-007	AB	1	`c0c555d07b60…`
2019-12-14 00:12 UTC	2019-12	N020658-001	AB	1	`3f01610625f2…`
2019-12-14 00:12 UTC	2019-12	N020658-002	AB	1	`3f01610625f2…`
2019-12-14 00:12 UTC	2019-12	N020658-003	AB	1	`3f01610625f2…`
2019-12-14 00:12 UTC	2019-12	N020658-004	AB	1	`3f01610625f2…`
2019-12-14 00:12 UTC	2019-12	N020658-005	AB	1	`3f01610625f2…`

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
0007-4896-20	EA - Each	0007-4896	a1e4b298-bb8d-41e5-b6ac-c59c7d3a246e	1	2012-07-24

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
ROPINIROLE HYDROCHLORIDE	ACTIVE INGREDIENT	D7ZD41RZI9	REQUIP (ROPINIROLE) TABLET, FILM COATED [GLAXOSMITHKLINE LLC]	9
ROPINIROLE	ACTIVE MOIETY	030PYR8953	REQUIP (ROPINIROLE) TABLET, FILM COATED [GLAXOSMITHKLINE LLC]	9
ALUMINUM OXIDE	INACTIVE INGREDIENT	LMI26O6933	REQUIP (ROPINIROLE) TABLET, FILM COATED [GLAXOSMITHKLINE LLC]	9
CELLULOSE, MICROCRYSTALLINE	INACTIVE INGREDIENT	OP1R32D61U	REQUIP (ROPINIROLE) TABLET, FILM COATED [GLAXOSMITHKLINE LLC]	9
COCHINEAL	INACTIVE INGREDIENT	TZ8Z31B35M	REQUIP (ROPINIROLE) TABLET, FILM COATED [GLAXOSMITHKLINE LLC]	9
CROSCARMELLOSE SODIUM	INACTIVE INGREDIENT	M28OL1HH48	REQUIP (ROPINIROLE) TABLET, FILM COATED [GLAXOSMITHKLINE LLC]	9
FD&C BLUE NO. 2	INACTIVE INGREDIENT	L06K8R7DQK	REQUIP (ROPINIROLE) TABLET, FILM COATED [GLAXOSMITHKLINE LLC]	9
FD&C YELLOW NO. 6	INACTIVE INGREDIENT	H77VEI93A8	REQUIP (ROPINIROLE) TABLET, FILM COATED [GLAXOSMITHKLINE LLC]	9
FERRIC OXIDE RED	INACTIVE INGREDIENT	1K09F3G675	REQUIP (ROPINIROLE) TABLET, FILM COATED [GLAXOSMITHKLINE LLC]	9
FERRIC OXIDE YELLOW	INACTIVE INGREDIENT	EX438O2MRT	REQUIP (ROPINIROLE) TABLET, FILM COATED [GLAXOSMITHKLINE LLC]	9
HYPROMELLOSE 2910 (3 MPA.S)	INACTIVE INGREDIENT	0VUT3PMY82	REQUIP (ROPINIROLE) TABLET, FILM COATED [GLAXOSMITHKLINE LLC]	9
HYPROMELLOSE 2910 (6 MPA.S)	INACTIVE INGREDIENT	0WZ8WG20P6	REQUIP (ROPINIROLE) TABLET, FILM COATED [GLAXOSMITHKLINE LLC]	9
INDIGOTINDISULFONATE SODIUM	INACTIVE INGREDIENT	D3741U8K7L	REQUIP (ROPINIROLE) TABLET, FILM COATED [GLAXOSMITHKLINE LLC]	9
LACTOSE MONOHYDRATE	INACTIVE INGREDIENT	EWQ57Q8I5X	REQUIP (ROPINIROLE) TABLET, FILM COATED [GLAXOSMITHKLINE LLC]	9
MAGNESIUM STEARATE	INACTIVE INGREDIENT	70097M6I30	REQUIP (ROPINIROLE) TABLET, FILM COATED [GLAXOSMITHKLINE LLC]	9
POLYETHYLENE GLYCOL 400	INACTIVE INGREDIENT	B697894SGQ	REQUIP (ROPINIROLE) TABLET, FILM COATED [GLAXOSMITHKLINE LLC]	9
POLYSORBATE 80	INACTIVE INGREDIENT	6OZP39ZG8H	REQUIP (ROPINIROLE) TABLET, FILM COATED [GLAXOSMITHKLINE LLC]	9
TITANIUM DIOXIDE	INACTIVE INGREDIENT	15FIX9V2JP	REQUIP (ROPINIROLE) TABLET, FILM COATED [GLAXOSMITHKLINE LLC]	9

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
D7ZD41RZI9	ROPINIROLE HYDROCHLORIDE	91374-20-8	ROPINIROLE HYDROCHLORIDE
030PYR8953	ROPINIROLE	91374-21-9	ropinirole