National Council for Prescription Drug Programs indexing - billing unit

Manufacturer: National Council for Prescription Drug Programs
Effective date: 2012-07-24
Label type: Indexing - Billing Unit
Version: 1
Source: full-release
Hydrated at: 2026-06-05 02:45:54

Label at a glance#

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
0007-4895-20	EA - Each	0007-4895	eaebe592-ebdd-449d-b0a8-e523d63bce0d	1	2012-07-24

NDC Codes#

Product NDC, Package NDC table
Product NDC	Package NDC
0007-4895	0007-4895-20

Source Document#

Source XML

Orange Book application contexts#

All distinct exact application/product contexts derived from this label’s complete NDC list are paginated below.

Orange Book application contexts page 1 of 1 · 1 matching rows.

Source provenance: Browse the complete Orange Book source catalog · source snapshot 44.

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REQUIP	ROPINIROLE HYDROCHLORIDE	EQ 0.25MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	1997-09-19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REQUIP	ROPINIROLE HYDROCHLORIDE	EQ 0.5MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	1997-09-19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REQUIP	ROPINIROLE HYDROCHLORIDE	EQ 1MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	1997-09-19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REQUIP	ROPINIROLE HYDROCHLORIDE	EQ 2MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	1997-09-19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REQUIP	ROPINIROLE HYDROCHLORIDE	EQ 5MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	1997-09-19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REQUIP	ROPINIROLE HYDROCHLORIDE	EQ 3MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	1999-01-27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REQUIP	ROPINIROLE HYDROCHLORIDE	EQ 4MG BASE Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD	1999-01-27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 · 308 observed states.

Captured, Edition, Application-product table
Captured	Edition	Application-product	Trade name	Strength	Dosage form / route	RLD / RS	Approval date	Source SHA-256
2026-10-15 13:18:30	2026-09	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	`c2088c7a36db…`
2026-10-15 13:18:30	2026-09	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	`c2088c7a36db…`
2026-10-15 13:18:30	2026-09	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	`c2088c7a36db…`
2026-10-15 13:18:30	2026-09	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	`c2088c7a36db…`
2026-10-15 13:18:30	2026-09	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	`c2088c7a36db…`
2026-10-15 13:18:30	2026-09	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	`c2088c7a36db…`
2026-10-15 13:18:30	2026-09	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	`c2088c7a36db…`
2026-09-14 22:38:34	2026-08	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	`84e616aacf4f…`
2026-09-14 22:38:34	2026-08	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	`84e616aacf4f…`
2026-09-14 22:38:34	2026-08	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	`84e616aacf4f…`
2026-09-14 22:38:34	2026-08	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	`84e616aacf4f…`
2026-09-14 22:38:34	2026-08	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	`84e616aacf4f…`
2026-09-14 22:38:34	2026-08	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	`84e616aacf4f…`
2026-09-14 22:38:34	2026-08	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	`84e616aacf4f…`
2026-08-18 06:07:40	2026-07	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	`caaa826d4ba7…`
2026-08-18 06:07:40	2026-07	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	`caaa826d4ba7…`
2026-08-18 06:07:40	2026-07	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	`caaa826d4ba7…`
2026-08-18 06:07:40	2026-07	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	`caaa826d4ba7…`
2026-08-18 06:07:40	2026-07	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	`caaa826d4ba7…`
2026-08-18 06:07:40	2026-07	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	`caaa826d4ba7…`
2026-08-18 06:07:40	2026-07	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	`caaa826d4ba7…`
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…`

Observed Orange Book normalized TE history#

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

Captured, Edition, Application-product table
Captured	Edition	Application-product	TE code	Order	Source SHA-256
2019-12-14 00:12 UTC	2019-12	N020658-006	AB	1	`3f01610625f2…`
2019-12-14 00:12 UTC	2019-12	N020658-007	AB	1	`3f01610625f2…`
2019-09-15 20:21 UTC	2019-09	N020658-001	AB	1	`b00525d2431f…`
2019-09-15 20:21 UTC	2019-09	N020658-002	AB	1	`b00525d2431f…`
2019-09-15 20:21 UTC	2019-09	N020658-003	AB	1	`b00525d2431f…`
2019-09-15 20:21 UTC	2019-09	N020658-004	AB	1	`b00525d2431f…`
2019-09-15 20:21 UTC	2019-09	N020658-005	AB	1	`b00525d2431f…`
2019-09-15 20:21 UTC	2019-09	N020658-006	AB	1	`b00525d2431f…`
2019-09-15 20:21 UTC	2019-09	N020658-007	AB	1	`b00525d2431f…`
2019-07-19 19:46 UTC	2019-07	N020658-001	AB	1	`ea99ee380514…`
2019-07-19 19:46 UTC	2019-07	N020658-002	AB	1	`ea99ee380514…`
2019-07-19 19:46 UTC	2019-07	N020658-003	AB	1	`ea99ee380514…`
2019-07-19 19:46 UTC	2019-07	N020658-004	AB	1	`ea99ee380514…`
2019-07-19 19:46 UTC	2019-07	N020658-005	AB	1	`ea99ee380514…`
2019-07-19 19:46 UTC	2019-07	N020658-006	AB	1	`ea99ee380514…`
2019-07-19 19:46 UTC	2019-07	N020658-007	AB	1	`ea99ee380514…`

Reported adverse events (FAERS/openFDA)#

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