Application 018017

Type: NDA
Sponsor: MERCK

Application Products#

Product, Drug, Ingredient table
Product	Drug	Ingredient	Form	Strength	Reference drug	Reference standard
001	BLOCADREN	TIMOLOL MALEATE	TABLET;ORAL	5MG Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons	Yes	No
002	BLOCADREN	TIMOLOL MALEATE	TABLET;ORAL	10MG Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons	Yes	No
004	BLOCADREN	TIMOLOL MALEATE	TABLET;ORAL	20MG Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons	Yes	No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 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	RLD / RS
N018017-001	BLOCADREN	TIMOLOL MALEATE	5MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD, Approved before 1982
N018017-002	BLOCADREN	TIMOLOL MALEATE	10MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD, Approved before 1982
N018017-004	BLOCADREN	TIMOLOL MALEATE	20MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD, Approved before 1982

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	RLD / RS	Source SHA-256
2024-08-13 05:28 UTC · 3 captures of this ZIP	2024-08	N018017-002	BLOCADREN	10MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD, Approved before 1982	`79d66fd596c7…`
2024-08-13 05:28 UTC · 3 captures of this ZIP	2024-08	N018017-004	BLOCADREN	20MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD, Approved before 1982	`79d66fd596c7…`
2024-07-13 05:37 UTC · 2 captures of this ZIP	2024-07	N018017-001	BLOCADREN	5MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD, Approved before 1982	`301d65b070ca…`
2024-07-13 05:37 UTC · 2 captures of this ZIP	2024-07	N018017-002	BLOCADREN	10MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD, Approved before 1982	`301d65b070ca…`
2024-07-13 05:37 UTC · 2 captures of this ZIP	2024-07	N018017-004	BLOCADREN	20MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD, Approved before 1982	`301d65b070ca…`
2024-06-18 03:08 UTC · 5 captures of this ZIP	2024-06	N018017-001	BLOCADREN	5MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD, Approved before 1982	`1e350fbaab3a…`
2024-06-18 03:08 UTC · 5 captures of this ZIP	2024-06	N018017-002	BLOCADREN	10MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD, Approved before 1982	`1e350fbaab3a…`
2024-06-18 03:08 UTC · 5 captures of this ZIP	2024-06	N018017-004	BLOCADREN	20MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD, Approved before 1982	`1e350fbaab3a…`
2024-05-31 18:47 UTC	2024-05	N018017-001	BLOCADREN	5MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD, Approved before 1982	`8072bd15b7f6…`
2024-05-31 18:47 UTC	2024-05	N018017-002	BLOCADREN	10MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD, Approved before 1982	`8072bd15b7f6…`
2024-05-31 18:47 UTC	2024-05	N018017-004	BLOCADREN	20MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD, Approved before 1982	`8072bd15b7f6…`
2022-06-29 02:47 UTC · 2 captures of this ZIP	2022-06	N018017-001	BLOCADREN	5MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD, Approved before 1982	`5c6f7cd8ea54…`
2022-06-29 02:47 UTC · 2 captures of this ZIP	2022-06	N018017-002	BLOCADREN	10MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD, Approved before 1982	`5c6f7cd8ea54…`
2022-06-29 02:47 UTC · 2 captures of this ZIP	2022-06	N018017-004	BLOCADREN	20MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD, Approved before 1982	`5c6f7cd8ea54…`
2022-04-08 23:34 UTC	2022-04	N018017-001	BLOCADREN	5MG	TABLET / ORAL	RLD, Approved before 1982	`5d02ea3f76ae…`
2022-04-08 23:34 UTC	2022-04	N018017-002	BLOCADREN	10MG	TABLET / ORAL	RLD, Approved before 1982	`5d02ea3f76ae…`
2022-04-08 23:34 UTC	2022-04	N018017-004	BLOCADREN	20MG	TABLET / ORAL	RLD, Approved before 1982	`5d02ea3f76ae…`
2022-04-04 05:41 UTC	2022-04	N018017-001	BLOCADREN	5MG	TABLET / ORAL	RLD, Approved before 1982	`4b0b4de00fa7…`
2022-04-04 05:41 UTC	2022-04	N018017-002	BLOCADREN	10MG	TABLET / ORAL	RLD, Approved before 1982	`4b0b4de00fa7…`
2022-04-04 05:41 UTC	2022-04	N018017-004	BLOCADREN	20MG	TABLET / ORAL	RLD, Approved before 1982	`4b0b4de00fa7…`
2019-12-13 00:20 UTC	2019-12	N018017-001	BLOCADREN	5MG Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons	TABLET / ORAL	RLD, Approved before 1982	`74a2ff9319b5…`
2019-12-13 00:20 UTC	2019-12	N018017-002	BLOCADREN	10MG Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons	TABLET / ORAL	RLD, Approved before 1982	`74a2ff9319b5…`
2019-12-13 00:20 UTC	2019-12	N018017-004	BLOCADREN	20MG Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons	TABLET / ORAL	RLD, Approved before 1982	`74a2ff9319b5…`
2022-03-09 01:35 UTC	2022-03	N018017-001	BLOCADREN	5MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD, Approved before 1982	`bb7c543d1eb4…`
2022-03-09 01:35 UTC	2022-03	N018017-002	BLOCADREN	10MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD, Approved before 1982	`bb7c543d1eb4…`
2022-03-09 01:35 UTC	2022-03	N018017-004	BLOCADREN	20MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	TABLET / ORAL	RLD, Approved before 1982	`bb7c543d1eb4…`
2021-12-28 21:50 UTC	2021-12	N018017-001	BLOCADREN	5MG Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons	TABLET / ORAL	RLD, Approved before 1982	`782e0a99824c…`
2021-12-28 21:50 UTC	2021-12	N018017-002	BLOCADREN	10MG Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons	TABLET / ORAL	RLD, Approved before 1982	`782e0a99824c…`
2021-12-28 21:50 UTC	2021-12	N018017-004	BLOCADREN	20MG Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons	TABLET / ORAL	RLD, Approved before 1982	`782e0a99824c…`
2021-05-05 16:15 UTC · 3 captures of this ZIP	2021-05	N018017-001	BLOCADREN	5MG Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons	TABLET / ORAL	RLD, Approved before 1982	`87673890dc5c…`
2021-05-05 16:15 UTC · 3 captures of this ZIP	2021-05	N018017-002	BLOCADREN	10MG Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons	TABLET / ORAL	RLD, Approved before 1982	`87673890dc5c…`
2021-05-05 16:15 UTC · 3 captures of this ZIP	2021-05	N018017-004	BLOCADREN	20MG Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons	TABLET / ORAL	RLD, Approved before 1982	`87673890dc5c…`
2021-03-12 10:30 UTC	2021-03	N018017-001	BLOCADREN	5MG Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons	TABLET / ORAL	RLD, Approved before 1982	`5aa47cf7b7d7…`
2021-03-12 10:30 UTC	2021-03	N018017-002	BLOCADREN	10MG Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons	TABLET / ORAL	RLD, Approved before 1982	`5aa47cf7b7d7…`
2021-03-12 10:30 UTC	2021-03	N018017-004	BLOCADREN	20MG Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons	TABLET / ORAL	RLD, Approved before 1982	`5aa47cf7b7d7…`
2020-12-22 03:56 UTC	2020-12	N018017-001	BLOCADREN	5MG Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons	TABLET / ORAL	RLD, Approved before 1982	`8869cabd3fbd…`
2020-12-22 03:56 UTC	2020-12	N018017-002	BLOCADREN	10MG Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons	TABLET / ORAL	RLD, Approved before 1982	`8869cabd3fbd…`
2020-12-22 03:56 UTC	2020-12	N018017-004	BLOCADREN	20MG Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons	TABLET / ORAL	RLD, Approved before 1982	`8869cabd3fbd…`
2020-11-12 02:37 UTC	2020-11	N018017-001	BLOCADREN	5MG Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons	TABLET / ORAL	RLD, Approved before 1982	`c0c555d07b60…`
2020-11-12 02:37 UTC	2020-11	N018017-002	BLOCADREN	10MG Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons	TABLET / ORAL	RLD, Approved before 1982	`c0c555d07b60…`

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 1 of 2 · 31 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
TIMOLOL MALEATE	TIMOLOL MALEATE	A-S Medication Solutions	64561dfd-3704-4820-aef6-d0d26cef7255	2026-09-02	Warnings, Adverse reactions	Name fallback generic name: TIMOLOL MALEATE
Timoptic in Ocudose	TIMOLOL MALEATE	Nordic Pharma, Inc.	16323b0e-78ae-40e5-be93-04f698dd672b	2026-08-06	Warnings, Adverse reactions	Name fallback generic name: TIMOLOL MALEATE
Timolol Maleate	TIMOLOL MALEATE	Sandoz Inc	f949fa34-6a9a-40d5-91ab-ff1cbb79b9ea	2026-02-20	Warnings, Adverse reactions	Name fallback generic name: TIMOLOL MALEATE
Timolol Maleate	TIMOLOL MALEATE	Sagent Pharmaceuticals	272bb565-f099-4896-b2f6-48ab9180e941	2026-01-09	Warnings, Adverse reactions	Name fallback generic name: TIMOLOL MALEATE
Timolol Maleate	TIMOLOL MALEATE	A-S Medication Solutions	7a1ea848-5b55-4038-afb1-029645ee0925	2025-12-30	Warnings, Adverse reactions	Name fallback generic name: TIMOLOL MALEATE
TIMOLOL MALEATE	TIMOLOL MALEATE	Rising Pharma Holdings, Inc.	2ed21930-1e05-46de-8acd-cb6f4798a7fa	2025-12-15	Warnings, Adverse reactions	Name fallback generic name: TIMOLOL MALEATE
Timolol maleate	TIMOLOL MALEATE	Armas Pharmaceuticals, Inc.	ea585fe8-3356-4f08-8078-34e8ab5de37e	2025-12-03	Warnings, Adverse reactions	Name fallback generic name: TIMOLOL MALEATE
Timolol Maleate	TIMOLOL MALEATE	Bausch & Lomb Americas Inc.	581f80f7-4419-49e2-867d-40443c75409f	2025-03-26	Warnings, Adverse reactions	Name fallback generic name: TIMOLOL MALEATE
Timolol Maleate	TIMOLOL MALEATE	Bausch & Lomb Americas Inc.	036dc753-1698-4c69-9bcf-752c7061203c	2025-03-05	Warnings, Adverse reactions	Name fallback generic name: TIMOLOL MALEATE
Timolol Maleate	TIMOLOL MALEATE	Bausch & Lomb Americas Inc.	9c14ca2d-80f3-48ef-b99a-beafaa728a24	2025-03-04	Warnings, Adverse reactions	Name fallback generic name: TIMOLOL MALEATE
Timolol Maleate	TIMOLOL MALEATE	A-S Medication Solutions	5305a38e-d9c8-4f9e-bf67-b246abc82cb1	2024-12-20	Warnings, Adverse reactions	Name fallback generic name: TIMOLOL MALEATE
Timolol Maleate	TIMOLOL MALEATE	Micro Labs Limited	79b223e4-d929-4667-8149-e79bfab13fdf	2024-12-05	Warnings, Adverse reactions	Name fallback generic name: TIMOLOL MALEATE
Timolol Maleate	TIMOLOL MALEATE	Bausch & Lomb Americas Inc.	b686bbad-1ef7-4b94-a316-4d182a40b89a	2024-11-04	Warnings, Adverse reactions	Name fallback generic name: TIMOLOL MALEATE
Timolol Maleate	TIMOLOL MALEATE	Somerset Therapeutics, LLC	e797f7c7-0588-4627-b060-8df6bcfe3f7b	2024-10-31	Warnings, Adverse reactions	Name fallback generic name: TIMOLOL MALEATE
Istalol	TIMOLOL MALEATE	Bausch & Lomb Incorporated	258bbc8d-00ee-45b0-ac35-6f16c4e8d45f	2024-10-30	Warnings, Adverse reactions	Name fallback generic name: TIMOLOL MALEATE
TIMOLOL MALEATE	TIMOLOL MALEATE	Leading Pharma, LLC	d6fa2971-dacf-42ab-99bc-c7ce6013221e	2024-10-30	Warnings, Adverse reactions	Name fallback generic name: TIMOLOL MALEATE
timolol maleate	TIMOLOL MALEATE	NorthStar RxLLC	9db7322d-eb31-4fff-9b14-8a0294d01704	2024-10-14	Warnings, Adverse reactions	Name fallback generic name: TIMOLOL MALEATE
Timolol Maleate	TIMOLOL MALEATE	Caplin Steriles Limited	4847f180-45e6-40f0-ae8c-6cc500cb0add	2024-08-19	Warnings, Adverse reactions	Name fallback generic name: TIMOLOL MALEATE
Timolol maleate	TIMOLOL MALEATE	Somerset Therapeutics, LLC	5d60db57-ca24-4cab-a90d-8cf06992a34e	2024-07-04	Warnings, Adverse reactions	Name fallback generic name: TIMOLOL MALEATE
Timolol Maleate	TIMOLOL MALEATE	Rising Pharma Holdings, Inc.	0bc40b2c-65eb-4095-87e6-4752d5b19a3a	2024-06-11	Warnings, Adverse reactions	Name fallback generic name: TIMOLOL MALEATE

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
20102	SUPPL	2003-07-05
785	SUPPL	2003-03-10
40771	SUPPL	2002-05-30
13981	SUPPL	2002-03-27