Application 020729

Type: NDA
Sponsor: UCB INC

Application Products#

Product, Drug, Ingredient table
Product	Drug	Ingredient	Form	Strength	Reference drug	Reference standard
001	UNIRETIC	HYDROCHLOROTHIAZIDE; MOEXIPRIL HYDROCHLORIDE	TABLET;ORAL	12.5MG;7.5MG Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons	No	No
002	UNIRETIC	HYDROCHLOROTHIAZIDE; MOEXIPRIL HYDROCHLORIDE	TABLET;ORAL	25MG;15MG Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons	No	No
003	UNIRETIC	HYDROCHLOROTHIAZIDE; MOEXIPRIL HYDROCHLORIDE	TABLET;ORAL	12.5MG;15MG Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons	No	No

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

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	Approval date
N020729-001	UNIRETIC	HYDROCHLOROTHIAZIDE; MOEXIPRIL HYDROCHLORIDE	12.5MG;7.5MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	1997-06-27
N020729-002	UNIRETIC	HYDROCHLOROTHIAZIDE; MOEXIPRIL HYDROCHLORIDE	25MG;15MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	1997-06-27
N020729-003	UNIRETIC	HYDROCHLOROTHIAZIDE; MOEXIPRIL HYDROCHLORIDE	12.5MG;15MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	2002-02-14

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 2 of 4 · 132 observed states.

Captured, Edition, Application-product table
Captured	Edition	Application-product	Trade name	Strength	Dosage form / route	Approval date	Source SHA-256
2024-08-13 05:28 UTC · 3 captures of this ZIP	2024-08	N020729-002	UNIRETIC	25MG;15MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	1997-06-27	`79d66fd596c7…`
2024-08-13 05:28 UTC · 3 captures of this ZIP	2024-08	N020729-003	UNIRETIC	12.5MG;15MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	2002-02-14	`79d66fd596c7…`
2024-07-13 05:37 UTC · 2 captures of this ZIP	2024-07	N020729-001	UNIRETIC	12.5MG;7.5MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	1997-06-27	`301d65b070ca…`
2024-07-13 05:37 UTC · 2 captures of this ZIP	2024-07	N020729-002	UNIRETIC	25MG;15MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	1997-06-27	`301d65b070ca…`
2024-07-13 05:37 UTC · 2 captures of this ZIP	2024-07	N020729-003	UNIRETIC	12.5MG;15MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	2002-02-14	`301d65b070ca…`
2024-06-18 03:08 UTC · 5 captures of this ZIP	2024-06	N020729-001	UNIRETIC	12.5MG;7.5MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	1997-06-27	`1e350fbaab3a…`
2024-06-18 03:08 UTC · 5 captures of this ZIP	2024-06	N020729-002	UNIRETIC	25MG;15MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	1997-06-27	`1e350fbaab3a…`
2024-06-18 03:08 UTC · 5 captures of this ZIP	2024-06	N020729-003	UNIRETIC	12.5MG;15MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	2002-02-14	`1e350fbaab3a…`
2024-05-31 18:47 UTC	2024-05	N020729-001	UNIRETIC	12.5MG;7.5MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	1997-06-27	`8072bd15b7f6…`
2024-05-31 18:47 UTC	2024-05	N020729-002	UNIRETIC	25MG;15MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	1997-06-27	`8072bd15b7f6…`
2024-05-31 18:47 UTC	2024-05	N020729-003	UNIRETIC	12.5MG;15MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	2002-02-14	`8072bd15b7f6…`
2022-06-29 02:47 UTC · 2 captures of this ZIP	2022-06	N020729-001	UNIRETIC	12.5MG;7.5MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	1997-06-27	`5c6f7cd8ea54…`
2022-06-29 02:47 UTC · 2 captures of this ZIP	2022-06	N020729-002	UNIRETIC	25MG;15MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	1997-06-27	`5c6f7cd8ea54…`
2022-06-29 02:47 UTC · 2 captures of this ZIP	2022-06	N020729-003	UNIRETIC	12.5MG;15MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	2002-02-14	`5c6f7cd8ea54…`
2022-04-08 23:34 UTC	2022-04	N020729-001	UNIRETIC	12.5MG;7.5MG	TABLET / ORAL	1997-06-27	`5d02ea3f76ae…`
2022-04-08 23:34 UTC	2022-04	N020729-002	UNIRETIC	25MG;15MG	TABLET / ORAL	1997-06-27	`5d02ea3f76ae…`
2022-04-08 23:34 UTC	2022-04	N020729-003	UNIRETIC	12.5MG;15MG	TABLET / ORAL	2002-02-14	`5d02ea3f76ae…`
2022-04-04 05:41 UTC	2022-04	N020729-001	UNIRETIC	12.5MG;7.5MG	TABLET / ORAL	1997-06-27	`4b0b4de00fa7…`
2022-04-04 05:41 UTC	2022-04	N020729-002	UNIRETIC	25MG;15MG	TABLET / ORAL	1997-06-27	`4b0b4de00fa7…`
2022-04-04 05:41 UTC	2022-04	N020729-003	UNIRETIC	12.5MG;15MG	TABLET / ORAL	2002-02-14	`4b0b4de00fa7…`
2019-12-13 00:20 UTC	2019-12	N020729-001	UNIRETIC	12.5MG;7.5MG Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons	TABLET / ORAL	1997-06-27	`74a2ff9319b5…`
2019-12-13 00:20 UTC	2019-12	N020729-002	UNIRETIC	25MG;15MG Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons	TABLET / ORAL	1997-06-27	`74a2ff9319b5…`
2019-12-13 00:20 UTC	2019-12	N020729-003	UNIRETIC	12.5MG;15MG Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons	TABLET / ORAL	2002-02-14	`74a2ff9319b5…`
2022-03-09 01:35 UTC	2022-03	N020729-001	UNIRETIC	12.5MG;7.5MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	1997-06-27	`bb7c543d1eb4…`
2022-03-09 01:35 UTC	2022-03	N020729-002	UNIRETIC	25MG;15MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	1997-06-27	`bb7c543d1eb4…`
2022-03-09 01:35 UTC	2022-03	N020729-003	UNIRETIC	12.5MG;15MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	2002-02-14	`bb7c543d1eb4…`
2021-12-28 21:50 UTC	2021-12	N020729-001	UNIRETIC	12.5MG;7.5MG Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons	TABLET / ORAL	1997-06-27	`782e0a99824c…`
2021-12-28 21:50 UTC	2021-12	N020729-002	UNIRETIC	25MG;15MG Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons	TABLET / ORAL	1997-06-27	`782e0a99824c…`
2021-12-28 21:50 UTC	2021-12	N020729-003	UNIRETIC	12.5MG;15MG Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons	TABLET / ORAL	2002-02-14	`782e0a99824c…`
2021-05-05 16:15 UTC · 3 captures of this ZIP	2021-05	N020729-001	UNIRETIC	12.5MG;7.5MG Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons	TABLET / ORAL	1997-06-27	`87673890dc5c…`
2021-05-05 16:15 UTC · 3 captures of this ZIP	2021-05	N020729-002	UNIRETIC	25MG;15MG Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons	TABLET / ORAL	1997-06-27	`87673890dc5c…`
2021-05-05 16:15 UTC · 3 captures of this ZIP	2021-05	N020729-003	UNIRETIC	12.5MG;15MG Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons	TABLET / ORAL	2002-02-14	`87673890dc5c…`
2021-03-12 10:30 UTC	2021-03	N020729-001	UNIRETIC	12.5MG;7.5MG Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons	TABLET / ORAL	1997-06-27	`5aa47cf7b7d7…`
2021-03-12 10:30 UTC	2021-03	N020729-002	UNIRETIC	25MG;15MG Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons	TABLET / ORAL	1997-06-27	`5aa47cf7b7d7…`
2021-03-12 10:30 UTC	2021-03	N020729-003	UNIRETIC	12.5MG;15MG Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons	TABLET / ORAL	2002-02-14	`5aa47cf7b7d7…`
2020-12-22 03:56 UTC	2020-12	N020729-001	UNIRETIC	12.5MG;7.5MG Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons	TABLET / ORAL	1997-06-27	`8869cabd3fbd…`
2020-12-22 03:56 UTC	2020-12	N020729-002	UNIRETIC	25MG;15MG Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons	TABLET / ORAL	1997-06-27	`8869cabd3fbd…`
2020-12-22 03:56 UTC	2020-12	N020729-003	UNIRETIC	12.5MG;15MG Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons	TABLET / ORAL	2002-02-14	`8869cabd3fbd…`
2020-11-12 02:37 UTC	2020-11	N020729-001	UNIRETIC	12.5MG;7.5MG Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons	TABLET / ORAL	1997-06-27	`c0c555d07b60…`
2020-11-12 02:37 UTC	2020-11	N020729-002	UNIRETIC	25MG;15MG Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons	TABLET / ORAL	1997-06-27	`c0c555d07b60…`

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
25652	SUPPL	2012-09-17
35246	SUPPL	2012-09-14
35245	SUPPL	2012-01-23
3220	SUPPL	2012-01-23
13305	SUPPL	2011-09-02
25651	SUPPL	2011-08-26
35244	SUPPL	2011-05-23
35243	SUPPL	2010-01-20
25650	SUPPL	2010-01-15
20885	SUPPL	2007-09-26
25649	SUPPL	2003-11-25
3219	SUPPL	2002-02-14