Application 070626

Type: ANDA
Sponsor: BAYER

Application Products#

Product, Drug, Ingredient table
Product	Drug	Ingredient	Form	Strength	Reference drug	Reference standard
001	MIDOL	IBUPROFEN	CAPSULE;ORAL	200MG Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons	No	No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 43.

Orange Book products#

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

Application-product, Trade name, Ingredient table
Application-product	Trade name	Ingredient	Strength	Dosage form / route	TE codes	RLD / RS	Approval date
A070626-001	MIDOL	IBUPROFEN	200MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	CAPSULE / ORAL			1987-09-02

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 2 · 43 observed states.

Captured, Edition, Application-product table
Captured	Edition	Application-product	Trade name	Strength	Dosage form / route	Approval date	Source SHA-256
2026-09-14 22:38:34	2026-08	A070626-001	MIDOL	200MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	CAPSULE / ORAL	1987-09-02	`84e616aacf4f…`
2026-08-18 06:07:40	2026-07	A070626-001	MIDOL	200MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	CAPSULE / ORAL	1987-09-02	`caaa826d4ba7…`
2026-02-19 14:30 UTC	2026-02	A070626-001	MIDOL	200MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	CAPSULE / ORAL	1987-09-02	`011fe1cb6892…`
2025-12-14 10:44 UTC · 2 captures of this ZIP	2025-12	A070626-001	MIDOL	200MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	CAPSULE / ORAL	1987-09-02	`31067a03dcf5…`
2025-08-23 18:47 UTC	2025-08	A070626-001	MIDOL	200MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	CAPSULE / ORAL	1987-09-02	`6a471c1ec25d…`
2025-03-22 03:13 UTC · 3 captures of this ZIP	2025-03	A070626-001	MIDOL	200MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	CAPSULE / ORAL	1987-09-02	`fd3edfee7708…`
2025-02-26 10:13 UTC · 3 captures of this ZIP	2025-02	A070626-001	MIDOL	200MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	CAPSULE / ORAL	1987-09-02	`b8a1b40f171c…`
2025-01-19 17:59 UTC · 7 captures of this ZIP	2025-01	A070626-001	MIDOL	200MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	CAPSULE / ORAL	1987-09-02	`03ed91905a0d…`
2024-12-13 21:23 UTC · 2 captures of this ZIP	2024-12	A070626-001	MIDOL	200MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	CAPSULE / ORAL	1987-09-02	`2680178bc6a6…`
2024-09-14 05:58 UTC · 2 captures of this ZIP	2024-09	A070626-001	MIDOL	200MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	CAPSULE / ORAL	1987-09-02	`5bbf6a4d5a75…`
2024-11-08 22:44 UTC · 3 captures of this ZIP	2024-11	A070626-001	MIDOL	200MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	CAPSULE / ORAL	1987-09-02	`d8e5a09893c0…`
2024-10-29 15:01 UTC	2024-10	A070626-001	MIDOL	200MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	CAPSULE / ORAL	1987-09-02	`d06236e962d9…`
2024-08-13 05:28 UTC · 3 captures of this ZIP	2024-08	A070626-001	MIDOL	200MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	CAPSULE / ORAL	1987-09-02	`79d66fd596c7…`
2024-07-13 05:37 UTC · 2 captures of this ZIP	2024-07	A070626-001	MIDOL	200MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	CAPSULE / ORAL	1987-09-02	`301d65b070ca…`
2024-06-18 03:08 UTC · 5 captures of this ZIP	2024-06	A070626-001	MIDOL	200MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	CAPSULE / ORAL	1987-09-02	`1e350fbaab3a…`
2024-05-31 18:47 UTC	2024-05	A070626-001	MIDOL	200MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	CAPSULE / ORAL	1987-09-02	`8072bd15b7f6…`
2022-06-29 02:47 UTC · 2 captures of this ZIP	2022-06	A070626-001	MIDOL	200MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	CAPSULE / ORAL	1987-09-02	`5c6f7cd8ea54…`
2022-04-08 23:34 UTC	2022-04	A070626-001	MIDOL	200MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	CAPSULE / ORAL	1987-09-02	`5d02ea3f76ae…`
2022-04-04 05:41 UTC	2022-04	A070626-001	MIDOL	200MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	CAPSULE / ORAL	1987-09-02	`4b0b4de00fa7…`
2019-12-13 00:20 UTC	2019-12	A070626-001	MIDOL	200MG Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons	CAPSULE / ORAL	1987-09-02	`74a2ff9319b5…`
2022-03-09 01:35 UTC	2022-03	A070626-001	MIDOL	200MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	CAPSULE / ORAL	1987-09-02	`bb7c543d1eb4…`
2021-12-28 21:50 UTC	2021-12	A070626-001	MIDOL	200MG Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons	CAPSULE / ORAL	1987-09-02	`782e0a99824c…`
2021-05-05 16:15 UTC · 3 captures of this ZIP	2021-05	A070626-001	MIDOL	200MG Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons	CAPSULE / ORAL	1987-09-02	`87673890dc5c…`
2021-03-12 10:30 UTC	2021-03	A070626-001	MIDOL	200MG Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons	CAPSULE / ORAL	1987-09-02	`5aa47cf7b7d7…`
2020-12-22 03:56 UTC	2020-12	A070626-001	MIDOL	200MG Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons	CAPSULE / ORAL	1987-09-02	`8869cabd3fbd…`
2020-11-12 02:37 UTC	2020-11	A070626-001	MIDOL	200MG Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons	CAPSULE / ORAL	1987-09-02	`c0c555d07b60…`
2019-12-14 00:12 UTC	2019-12	A070626-001	MIDOL	200MG Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons	CAPSULE / ORAL	1987-09-02	`3f01610625f2…`
2019-09-15 20:21 UTC	2019-09	A070626-001	MIDOL	200MG Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons	CAPSULE / ORAL	1987-09-02	`b00525d2431f…`
2019-07-19 19:46 UTC	2019-07	A070626-001	MIDOL	200MG Federal Register determination that product was not discontinued or withdrawn for safety or efficacy reasons	CAPSULE / ORAL	1987-09-02	`ea99ee380514…`
2024-03-16 18:09 UTC · 4 captures of this ZIP	2024-03	A070626-001	MIDOL	200MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	CAPSULE / ORAL	1987-09-02	`6a51e52b5d6a…`
2024-02-18 07:12 UTC	2024-02	A070626-001	MIDOL	200MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	CAPSULE / ORAL	1987-09-02	`1c564ffb4f44…`
2023-12-20 04:57 UTC	2023-12	A070626-001	MIDOL	200MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	CAPSULE / ORAL	1987-09-02	`ea1830bbd6c7…`
2023-11-28 05:40 UTC · 2 captures of this ZIP	2023-11	A070626-001	MIDOL	200MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	CAPSULE / ORAL	1987-09-02	`a72a2bbeb626…`
2023-10-25 00:34 UTC · 2 captures of this ZIP	2023-10	A070626-001	MIDOL	200MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	CAPSULE / ORAL	1987-09-02	`9b2671bbb829…`
2023-07-15 15:27 UTC · 2 captures of this ZIP	2023-07	A070626-001	MIDOL	200MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	CAPSULE / ORAL	1987-09-02	`a67488948f0b…`
2023-06-13 01:57 UTC · 3 captures of this ZIP	2023-06	A070626-001	MIDOL	200MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	CAPSULE / ORAL	1987-09-02	`3f0d92c62455…`
2023-05-13 08:27 UTC	2023-05	A070626-001	MIDOL	200MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	CAPSULE / ORAL	1987-09-02	`053a50430f4f…`
2023-01-26 05:58 UTC	2023-01	A070626-001	MIDOL	200MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	CAPSULE / ORAL	1987-09-02	`3bdfa0b2c4d7…`
2022-11-12 20:34 UTC · 5 captures of this ZIP	2022-11	A070626-001	MIDOL	200MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	CAPSULE / ORAL	1987-09-02	`3a93d1ddd44b…`
2022-10-28 04:53 UTC	2022-10	A070626-001	MIDOL	200MG Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons	CAPSULE / ORAL	1987-09-02	`f41ea6bd6efb…`

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 35 of 46 · 918 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Ibuprofen	IBUPROFEN	Granules India Limited	fd01353d-1d1d-42b5-9a03-575052189bf5	2024-08-13	Warnings	Name fallback generic name: IBUPROFEN
Ibuprofen	IBUPROFEN	Florida Pharmaceutical Products, LLC	c1733fdb-5eed-2094-e053-2995a90a6c8e	2024-08-08	Boxed warning, Warnings, Adverse reactions	Name fallback generic name: IBUPROFEN
Ibuprofen	IBUPROFEN	Bryant Ranch Prepack	60f1c099-5fb5-47e8-b228-11de1ef40f4b	2024-08-08	Boxed warning, Warnings, Adverse reactions	Name fallback generic name: IBUPROFEN
Ibuprofen	IBUPROFEN	Bryant Ranch Prepack	ffc953f7-ed92-4528-bb2f-72c634c119fa	2024-08-08	Boxed warning, Warnings, Adverse reactions	Name fallback generic name: IBUPROFEN
Ibuprofen	IBUPROFEN	Advanced Rx of Tennessee, LLC	19b06eaf-0d4c-2b4d-e063-6294a90a2eb9	2024-08-06	Boxed warning, Warnings, Adverse reactions	Name fallback generic name: IBUPROFEN
Ibuprofen	IBUPROFEN	P & L Development, LLC	6d1c9a64-c83c-4b3d-9245-704b94cb367c	2024-07-30	Warnings	Name fallback generic name: IBUPROFEN
Ibuprofen	IBUPROFEN	Amneal Pharmaceuticals of New York LLC	faebc392-0fd9-4c71-8471-beba10dda022	2024-07-29	Boxed warning, Warnings, Adverse reactions	Name fallback generic name: IBUPROFEN
Ibuprofen	IBUPROFEN	Actavis Pharma, Inc.	3d156d13-25d8-4cfc-8285-5f7ebf48cf45	2024-07-24	Boxed warning, Warnings, Adverse reactions	Name fallback generic name: IBUPROFEN
IBU	IBUPROFEN	NuCare Pharmaceuticals,Inc.	678e2d16-33f3-67a7-e053-2991aa0a1132	2024-07-18	Boxed warning, Warnings, Adverse reactions	Name fallback generic name: IBUPROFEN
Ibuprofen	IBUPROFEN	Amneal Pharmaceuticals of New York LLC	75d963b9-3675-44ff-bc6b-83461bed1b67	2024-07-18	Boxed warning, Warnings, Adverse reactions	Name fallback generic name: IBUPROFEN
Ibuprofen	IBUPROFEN	Amneal Pharmaceuticals of New York LLC	57cdd1df-a303-4265-a2d6-1d0b87105a28	2024-07-18	Boxed warning, Warnings, Adverse reactions	Name fallback generic name: IBUPROFEN
Ibuprofen	IBUPROFEN	Amneal Pharmaceuticals of New York LLC	8df77ead-27eb-4f6f-95a9-f68d3e9cfa71	2024-07-18	Boxed warning, Warnings, Adverse reactions	Name fallback generic name: IBUPROFEN
IBUPROFEN	IBUPROFEN	NuCare Pharmaceuticals,Inc.	54b25106-5580-119d-e054-00144ff88e88	2024-07-17		Name fallback generic name: IBUPROFEN
ibuprofen	IBUPROFEN	Bryant Ranch Prepack	22cb2ccc-ba4d-4069-8334-f886f0e3e802	2024-07-12	Warnings	Name fallback generic name: IBUPROFEN
Foster and Thrive Infants Ibuprofen	IBUPROFEN	Strategic Sourcing Services LLC	fe3092af-9a7b-4189-af89-31be8d6fed53	2024-07-12	Warnings	Name fallback generic name: IBUPROFEN
Ibuprofen	IBUPROFEN	NuCare Pharmaceuticals,Inc.	92efad86-31ae-78e5-e053-2995a90a0fda	2024-07-03	Boxed warning, Warnings, Adverse reactions	Name fallback generic name: IBUPROFEN
Ibuprofen	IBUPROFEN	NuCare Pharmaceuticals, Inc.	3e3848f2-4922-39ea-e054-00144ff88e88	2024-06-25	Warnings	Name fallback generic name: IBUPROFEN
IBUPROFEN	IBUPROFEN	NuCare Pharmaceuticals,Inc.	999aa615-72b2-9296-e053-2a95a90ac70b	2024-06-20		Name fallback generic name: IBUPROFEN
IBUPROFEN	IBUPROFEN	NuCare Pharmaceuticals,Inc.	9973bfa2-693a-1165-e053-2995a90a4b1d	2024-06-20		Name fallback generic name: IBUPROFEN
IBUPROFEN	IBUPROFEN	NuCare Pharmaceuticals,Inc.	99d7cf65-3ec2-24eb-e053-2a95a90acc5e	2024-06-20		Name fallback generic name: IBUPROFEN

Reported adverse events (FAERS/openFDA)#

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