Ibuprofen

Product NDC: 72603-910
Requested package NDC: 72603-910-01
11-digit product format: 726030910
Labeler code: 72603
Product ID: 72603-910_aeee629b-255c-40d8-8e95-779aec00f723
Type: HUMAN PRESCRIPTION DRUG
Nonproprietary name: Ibuprofen
Dosage form: TABLET
Route: ORAL
Labeler: NorthStar Rx LLC
Application: ANDA213794
Marketing category: ANDA
Marketing start: 2026-06-01
Substance: IBUPROFEN
Active strength: 800 mg/1
Pharmacologic classes: Anti-Inflammatory Agents; Non-Steroidal [CS]; Cyclooxygenase Inhibitors [MoA]; Nonsteroidal Anti-inflammatory Drug [EPC]
Listing certified through: 2027-12-31
Current FDA listing: Yes

Source provenance: Browse the complete Orange Book source catalog · source snapshot 1.

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	TE codes	Approval date
A213794-001	IBUPROFEN	IBUPROFEN	400MG	TABLET / ORAL	AB	2020-05-08
A213794-002	IBUPROFEN	IBUPROFEN	600MG	TABLET / ORAL	AB	2020-05-08
A213794-003	IBUPROFEN	IBUPROFEN	800MG	TABLET / ORAL	AB	2020-05-08

Therapeutic equivalence codes#

Current TE-code rows page 1 of 1 · 3 matching rows.

Application-product, TE code table
Application-product	TE code
A213794-001	AB
A213794-002	AB
A213794-003	AB

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	Product TE source text	Approval date	Source SHA-256
2026-08-01 22:54:32	2026-06	A213794-001	IBUPROFEN	400MG	TABLET / ORAL	AB	2020-05-08	`a50c72e98297…`
2026-08-01 22:54:32	2026-06	A213794-002	IBUPROFEN	600MG	TABLET / ORAL	AB	2020-05-08	`a50c72e98297…`
2026-08-01 22:54:32	2026-06	A213794-003	IBUPROFEN	800MG	TABLET / ORAL	AB	2020-05-08	`a50c72e98297…`

Observed Orange Book normalized TE history#

Captured, Edition, Application-product table
Captured	Edition	Application-product	TE code	Order	Source SHA-256
2026-08-01 22:54:32	2026-06	A213794-001	AB	1	`a50c72e98297…`
2026-08-01 22:54:32	2026-06	A213794-002	AB	1	`a50c72e98297…`
2026-08-01 22:54:32	2026-06	A213794-003	AB	1	`a50c72e98297…`

openFDA label cross-check#

Cross-check layer: openFDA label JSON enriches search and identifies hydration gaps. The DailyMed Structured Product Label remains the canonical label presentation on FDA.report. Every label matching the complete exact-identifier union is deduplicated and paginated below.

Matched openFDA labels page 1 of 2 · 38 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Ibuprofen	IBUPROFEN	St. Mary's Medical Park Pharmacy	0a98cce4-f5c0-12a8-e063-6294a90a4e7e	2026-07-07	Boxed warning, Warnings, Adverse reactions	Exact identifier application applno (ANDA): 213794 application number: ANDA213794
Ibuprofen	IBUPROFEN	Proficient Rx LP	34a9b94f-93ba-4a7c-92eb-d0b4b530d887	2026-07-02	Boxed warning, Warnings, Adverse reactions	Exact identifier application applno (ANDA): 213794 application number: ANDA213794
Ibuprofen	IBUPROFEN	HAWAII REPACK, INC.	6239818c-747d-4cbb-9b41-27ca8bbce41b	2026-06-26	Boxed warning, Warnings, Adverse reactions	Exact identifier application applno (ANDA): 213794 application number: ANDA213794
Ibuprofen	IBUPROFEN	Sportpharm LLC	cef04ae4-e78a-454d-bb66-84b1d348c106	2026-06-26	Boxed warning, Warnings, Adverse reactions	Exact identifier application applno (ANDA): 213794 application number: ANDA213794
Ibuprofen	IBUPROFEN	Unit Dose Solutions, Inc.	5515e80f-7513-b425-e063-6294a90aa542	2026-06-25	Boxed warning, Warnings, Adverse reactions	Exact identifier application applno (ANDA): 213794 application number: ANDA213794
Ibuprofen	IBUPROFEN	REMEDYREPACK INC.	2fa4bfc8-386c-433b-bc46-24fc8ec1bca1	2026-06-12	Boxed warning, Warnings, Adverse reactions	Exact identifier application applno (ANDA): 213794 application number: ANDA213794
Ibuprofen	IBUPROFEN	REMEDYREPACK INC.	ec6b2df4-2f4f-4601-8b53-0542664e0bd9	2026-06-10	Boxed warning, Warnings, Adverse reactions	Exact identifier application applno (ANDA): 213794 application number: ANDA213794
Ibuprofen	IBUPROFEN	Preferred Pharmaceuticals Inc.	bdc3f482-6fba-4420-9118-0f5cb7744e97	2026-05-13	Boxed warning, Warnings, Adverse reactions	Exact identifier application applno (ANDA): 213794 application number: ANDA213794
Ibuprofen	IBUPROFEN	Preferred Pharmaceuticals Inc.	13fd4401-1821-4f2b-a44e-96aa2fa75b5c	2026-05-13	Boxed warning, Warnings, Adverse reactions	Exact identifier application applno (ANDA): 213794 application number: ANDA213794
Ibuprofen	IBUPROFEN	Preferred Pharmaceuticals Inc.	25d9f5fc-4d95-4018-add8-ba696b6079b2	2026-05-13	Boxed warning, Warnings, Adverse reactions	Exact identifier application applno (ANDA): 213794 application number: ANDA213794
Ibuprofen	IBUPROFEN	NuCare Pharmaceuticals,Inc.	05ce8e8e-0b25-061e-e063-6394a90a2e92	2026-05-07	Boxed warning, Warnings, Adverse reactions	Exact identifier application applno (ANDA): 213794 application number: ANDA213794
Ibuprofen	IBUPROFEN	Coupler LLC	50766a3d-1a22-be14-e063-6294a90a0ed2	2026-04-27	Boxed warning, Warnings, Adverse reactions	Exact identifier application applno (ANDA): 213794 application number: ANDA213794
Ibuprofen	IBUPROFEN	NorthStar Rx LLC	aeee629b-255c-40d8-8e95-779aec00f723	2026-03-18	Boxed warning, Warnings, Adverse reactions	Exact identifier application applno (ANDA): 213794 application number: ANDA213794 ndc (package): 72603-910-01 ndc (product): 72603-910 ndc11 (package): 72603091001
Ibuprofen	IBUPROFEN	Direct_Rx	1aa11b52-1aca-9219-e063-6294a90a470f	2026-03-05	Boxed warning, Warnings, Adverse reactions	Exact identifier application applno (ANDA): 213794 application number: ANDA213794
Ibuprofen	IBUPROFEN	A-S Medication Solutions	f24582be-8d70-4848-bd54-e55fa28f394f	2025-12-18	Boxed warning, Warnings, Adverse reactions	Exact identifier application applno (ANDA): 213794 application number: ANDA213794
Ibuprofen	IBUPROFEN	A-S Medication Solutions	e5db46f3-043b-40ac-a89b-c90bd562e7b4	2025-12-18	Boxed warning, Warnings, Adverse reactions	Exact identifier application applno (ANDA): 213794 application number: ANDA213794
Ibuprofen	IBUPROFEN	A-S Medication Solutions	3db0c659-cc43-45dc-8442-bc89093d94d7	2025-12-17	Boxed warning, Warnings, Adverse reactions	Exact identifier application applno (ANDA): 213794 application number: ANDA213794
Ibuprofen	IBUPROFEN	NuCare Pharmaceuticals,Inc.	f60445d3-807e-0bbf-e053-2995a90a1299	2025-10-30	Boxed warning, Warnings, Adverse reactions	Exact identifier application applno (ANDA): 213794 application number: ANDA213794
Ibuprofen	IBUPROFEN	A-S Medication Solutions	8d5f7d2a-af48-4d47-8bf5-48f01c092d24	2025-10-27	Boxed warning, Warnings, Adverse reactions	Exact identifier application applno (ANDA): 213794 application number: ANDA213794
Ibuprofen	IBUPROFEN	A-S Medication Solutions	4b75bd6f-5455-4237-991c-eacc0fdcf709	2025-10-27	Boxed warning, Warnings, Adverse reactions	Exact identifier application applno (ANDA): 213794 application number: ANDA213794

Additional Listing Data#

Finished product: Yes
Brand name base: Ibuprofen
Listing expiration: 2027-12-31

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
IBUPROFEN	800 mg/1

Harmonized UNII identifiers#

UNII identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
WK2XYI10QM	Internal UNII lookup

Harmonized RxCUI identifiers#

RxCUI identifiers page 1 of 1 · 2 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
197806	Internal RxNorm lookup
197807	Internal RxNorm lookup

Harmonized SPL set identifiers#

SPL set identifiers page 1 of 1 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
aeee629b-255c-40d8-8e95-779aec00f723	Available on FDA.report

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
1e73f975-1ce7-705e-2bcf-788b1b5e24ba	Product name	5	20251124
362d7abb-94e6-4c60-9a58-266894157713	Product name	1	20231023
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
816b97af-edc5-4060-aff1-b814bdbcad50	Product name	1	20190415
419aab54-5d5a-4146-9453-026d4a9991be	Product name	2	20170525
557673c2-8256-b351-e863-4ec71a5a64b0	Product name	2	20160714
dbc9a339-6215-4e94-9546-57a3b34902ce	Product name	1	20160517
89dac932-b90a-4410-9ab1-84c53e57de25	Product name	1	20150316
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
d723478e-ad4a-ec23-6bd7-cfe33e1e3840	Product name	1	20140508

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

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Sample	Status
72603-910-01	72603091001	100 TABLET in 1 BOTTLE (72603-910-01)	100 tablet	2026-06-01	0	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
Ibuprofen Tablets, USP Rx only	NorthStar Rx LLC \| Aurobindo Pharma Limited \| APL HEALTHCARE LIMITED	2026-03-18	Human Prescription Drug Label	1