Ibuprofen

Product NDC: 11788-006
Requested package NDC: 11788-006-07
11-digit product format: 117880006
Labeler code: 11788
Product ID: 11788-006_76b47c18-02e3-524e-e053-2a91aa0adaec
Type: HUMAN OTC DRUG
Nonproprietary name: Ibuprofen
Dosage form: TABLET, FILM COATED
Route: ORAL
Labeler: AiPing Pharmaceutical, Inc.
Application: ANDA206990
Marketing category: ANDA
Marketing start: 2019-03-01
Marketing end: 0000-00-00
Substance: IBUPROFEN
Active strength: 200 mg/1
NDC exclude flag: No
Listing certified through: 2020-12-31
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 · 1 matching rows.

Dataset, Scope, Product NDC table
Dataset	Scope	Product NDC	Package NDC	Code	Status	Reporting period	Source date
excluded package	package	11788-006	11788-006-07	I	Inactivated by FDA		2026-08-17

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 · 15 matching rows.

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

Captured / source date, Snapshot, Source SHA-256 table
Captured / source date	Snapshot	Source SHA-256
2025-12-14 17:58 UTC · source 2025-12-05	`d630ba8d3edf…`	`732f749b63fb…`
2025-08-27 00:01 UTC · source 2025-08-26	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-04-01 02:39 UTC · source 2025-03-31	`2ef7874e63bc…`	`57b86245f4fa…`
2025-03-28 20:22 UTC · source 2025-03-28	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-22 03:12 UTC · source 2025-03-21	`cfe11265f3b6…`	`090c488252e2…`
2025-03-10 12:48 UTC · source 2025-03-10	`cdf11ea48f46…`	`ba0047e9e063…`
2025-02-02 03:52 UTC · source 2025-01-31	`302b2466d912…`	`e7b80fea0513…`
2025-01-20 13:05 UTC · source 2025-01-20	`ed331223b511…`	`672a5bd82f5f…`
2025-01-11 03:41 UTC · source 2025-01-10	`0efc9e666f02…`	`f202fb6c5f17…`
2024-11-09 02:27 UTC · source 2024-11-08	`ad56d346431e…`	`cc804d4bbf1e…`
2024-10-04 04:10 UTC · source 2024-10-03	`367a005e9d99…`	`383a685ebd0f…`
2024-07-10 04:00 UTC · source 2024-07-09	`557ba5c1ecfa…`	`9c80585c8c6e…`
2024-05-28 21:12 UTC · source 2024-05-28	`8af77b9d5b6f…`	`d9bbb34c5368…`
2024-05-15 03:39 UTC · source 2024-05-14	`834df4deac94…`	`adcc014656a3…`
2024-03-11 06:39 UTC · source 2024-03-08	`1332a3947898…`	`d4bfe170f9cd…`

Source provenance: Browse the complete Orange Book source catalog.

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.

Captured, Edition, Application-product table
Captured	Edition	Application-product	Trade name	Strength	Dosage form / route	Approval date	Source SHA-256
2019-12-13 00:20 UTC	2019-12	A206990-001	IBUPROFEN	200MG	TABLET / ORAL	2018-08-21	`74a2ff9319b5…`
2019-12-14 00:12 UTC	2019-12	A206990-001	IBUPROFEN	200MG	TABLET / ORAL	2018-08-21	`3f01610625f2…`
2019-09-15 20:21 UTC	2019-09	A206990-001	IBUPROFEN	200MG	TABLET / ORAL	2018-08-21	`b00525d2431f…`
2019-07-19 19:46 UTC	2019-07	A206990-001	IBUPROFEN	200MG	TABLET / ORAL	2018-08-21	`ea99ee380514…`

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
1e73f975-1ce7-705e-2bcf-788b1b5e24ba	Product name	5	20251124
16cde546-8deb-4df2-a072-dab5566ede95	Product name	1	20231003
f6d1b8d7-3bd1-4248-eddd-b60565c88015	Product name	4	20230808
874f4e63-49d2-5150-5d77-052172814ebd	Product name	6	20230105
557673c2-8256-b351-e863-4ec71a5a64b0	Product name	2	20160714
dbc9a339-6215-4e94-9546-57a3b34902ce	Product name	1	20160517
61c18d4e-b552-5478-8fc0-df38b93e3100	Product name	1	20140508
7b2938c9-7eb7-e312-ae90-f54f4240361e	Product name	1	20140508
997601aa-bb5f-6971-6b90-a21132c12c7b	Product name	1	20140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
11788-006-00	2024-01-30	C162847	48780-1	1030e365-0e9c-111a-e063-dadaa90a10e2	IBUPROFEN ROUND TABLETS, USP 200mg
11788-006-07	2024-01-30	C162847	48780-1	1030e365-293f-111a-e063-dadaa90a10e2	Ibuprofen Tablets, USP 200 mg
11788-006-10	2024-01-30	C162847	48780-1	1030e365-293f-111a-e063-dadaa90a10e2	Ibuprofen Tablets, USP 200 mg

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
11788-006-07	Ibuprofen	24 in 1 BOTTLE	TABLET, FILM COATED	24	2
11788-006-07	Ibuprofen	1 in 1 CARTON	TABLET, FILM COATED	1	2
11788-006-10	Ibuprofen	1000 in 1 BOTTLE	TABLET, FILM COATED	1000	2
11788-006-00	Ibuprofen	50864 in 1 CARTON	TABLET, FILM COATED	50864	1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
11788-006	IBUPROFEN TABLET, FILM COATED [AIPING PHARMACEUTICAL, INC.]	2	Legacy NDC, 3 package rows	20190301_764ff65b-e6de-62e5-e053-2991aa0a94e5.zip
11788-006	IBUPROFEN TABLET, FILM COATED [AIPING PHARMACEUTICAL, INC.]	1	Legacy NDC, 1 package rows	20190301_76b47c18-02e2-524e-e053-2a91aa0adaec.zip

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
WK2XYI10QM	IBUPROFEN	15687-27-1	IBUPROFEN

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
310965	ibuprofen 200 MG Oral Tablet	PSN	764ff65b-e6de-62e5-e053-2991aa0a94e5	2
310965	ibuprofen 200 MG Oral Tablet	SCD	764ff65b-e6de-62e5-e053-2991aa0a94e5	2
310965	ibuprofen 200 MG (as ibuprofen sodium 256 MG) Oral Tablet	SY	764ff65b-e6de-62e5-e053-2991aa0a94e5	2
310965	ibuprofen 200 MG Oral Tablet	PSN	76b47c18-02e2-524e-e053-2a91aa0adaec	1
310965	ibuprofen 200 MG Oral Tablet	SCD	76b47c18-02e2-524e-e053-2a91aa0adaec	1
310965	ibuprofen 200 MG (as ibuprofen sodium 256 MG) Oral Tablet	SY	76b47c18-02e2-524e-e053-2a91aa0adaec	1

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
11788-006-07	11788000607	1 BOTTLE in 1 CARTON (11788-006-07) > 24 TABLET, FILM COATED in 1 BOTTLE	1 bottle	2019-03-01	0000-00-00	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
Ibuprofen Tablets, USP 200 mg	AiPing Pharmaceutical, Inc. \| Anshi Pharmaceutical (Zhongshan) Inc.	2018-12-06	HUMAN OTC DRUG LABEL	2
IBUPROFEN ROUND TABLETS, USP 200mg	AiPing Pharmaceutical, Inc. \| Anshi Pharmaceutical (Zhongshan) Inc.	2018-09-25	HUMAN OTC DRUG LABEL	1