Ibuprofen

Product NDC: 36800-221
Requested package NDC: 36800-221-11
11-digit product format: 368000221
Labeler code: 36800
Product ID: 36800-221_427c1aff-4849-1146-e063-6394a90ac0e9
Type: HUMAN OTC DRUG
Nonproprietary name: Ibuprofen
Dosage form: CAPSULE, LIQUID FILLED
Route: ORAL
Labeler: TOP CARE (Topco Associates LLC)
Application: ANDA078682
Marketing category: ANDA
Marketing start: 2021-08-18
Substance: IBUPROFEN
Active strength: 200 mg/1
Pharmacologic classes: Anti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Nonsteroidal Anti-inflammatory Drug [EPC]
NDC exclude flag: No
Listing certified through: 2026-12-31
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 · 1 matching rows.

Application-product, Trade name, Ingredient table
Application-product	Trade name	Ingredient	Strength	Dosage form / route	TE codes	RLD / RS	Approval date
A078682-001	IBUPROFEN	IBUPROFEN	EQ 200MG FREE ACID AND POTASSIUM SALT	CAPSULE / ORAL			2009-03-24

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 · 41 observed states.

Captured, Edition, Application-product table
Captured	Edition	Application-product	Trade name	Strength	Dosage form / route	Approval date	Source SHA-256
2026-02-19 14:30 UTC	2026-02	A078682-001	IBUPROFEN	EQ 200MG FREE ACID AND POTASSIUM SALT	CAPSULE / ORAL	2009-03-24	`011fe1cb6892…`
2025-12-14 10:44 UTC · 2 captures of this ZIP	2025-12	A078682-001	IBUPROFEN	EQ 200MG FREE ACID AND POTASSIUM SALT	CAPSULE / ORAL	2009-03-24	`31067a03dcf5…`
2025-08-23 18:47 UTC	2025-08	A078682-001	IBUPROFEN	EQ 200MG FREE ACID AND POTASSIUM SALT	CAPSULE / ORAL	2009-03-24	`6a471c1ec25d…`
2025-03-22 03:13 UTC · 3 captures of this ZIP	2025-03	A078682-001	IBUPROFEN	EQ 200MG FREE ACID AND POTASSIUM SALT	CAPSULE / ORAL	2009-03-24	`fd3edfee7708…`
2025-02-26 10:13 UTC · 3 captures of this ZIP	2025-02	A078682-001	IBUPROFEN	EQ 200MG FREE ACID AND POTASSIUM SALT	CAPSULE / ORAL	2009-03-24	`b8a1b40f171c…`
2025-01-19 17:59 UTC · 7 captures of this ZIP	2025-01	A078682-001	IBUPROFEN	EQ 200MG FREE ACID AND POTASSIUM SALT	CAPSULE / ORAL	2009-03-24	`03ed91905a0d…`
2024-12-13 21:23 UTC · 2 captures of this ZIP	2024-12	A078682-001	IBUPROFEN	EQ 200MG FREE ACID AND POTASSIUM SALT	CAPSULE / ORAL	2009-03-24	`2680178bc6a6…`
2024-09-14 05:58 UTC · 2 captures of this ZIP	2024-09	A078682-001	IBUPROFEN	EQ 200MG FREE ACID AND POTASSIUM SALT	CAPSULE / ORAL	2009-03-24	`5bbf6a4d5a75…`
2024-11-08 22:44 UTC · 3 captures of this ZIP	2024-11	A078682-001	IBUPROFEN	EQ 200MG FREE ACID AND POTASSIUM SALT	CAPSULE / ORAL	2009-03-24	`d8e5a09893c0…`
2024-10-29 15:01 UTC	2024-10	A078682-001	IBUPROFEN	EQ 200MG FREE ACID AND POTASSIUM SALT	CAPSULE / ORAL	2009-03-24	`d06236e962d9…`
2024-08-13 05:28 UTC · 3 captures of this ZIP	2024-08	A078682-001	IBUPROFEN	EQ 200MG FREE ACID AND POTASSIUM SALT	CAPSULE / ORAL	2009-03-24	`79d66fd596c7…`
2024-07-13 05:37 UTC · 2 captures of this ZIP	2024-07	A078682-001	IBUPROFEN	EQ 200MG FREE ACID AND POTASSIUM SALT	CAPSULE / ORAL	2009-03-24	`301d65b070ca…`
2024-06-18 03:08 UTC · 5 captures of this ZIP	2024-06	A078682-001	IBUPROFEN	EQ 200MG FREE ACID AND POTASSIUM SALT	CAPSULE / ORAL	2009-03-24	`1e350fbaab3a…`
2024-05-31 18:47 UTC	2024-05	A078682-001	IBUPROFEN	EQ 200MG FREE ACID AND POTASSIUM SALT	CAPSULE / ORAL	2009-03-24	`8072bd15b7f6…`
2022-06-29 02:47 UTC · 2 captures of this ZIP	2022-06	A078682-001	IBUPROFEN	EQ 200MG FREE ACID AND POTASSIUM SALT	CAPSULE / ORAL	2009-03-24	`5c6f7cd8ea54…`
2022-04-08 23:34 UTC	2022-04	A078682-001	IBUPROFEN	EQ 200MG FREE ACID AND POTASSIUM SALT	CAPSULE / ORAL	2009-03-24	`5d02ea3f76ae…`
2022-04-04 05:41 UTC	2022-04	A078682-001	IBUPROFEN	EQ 200MG FREE ACID AND POTASSIUM SALT	CAPSULE / ORAL	2009-03-24	`4b0b4de00fa7…`
2019-12-13 00:20 UTC	2019-12	A078682-001	IBUPROFEN	EQ 200MG FREE ACID AND POTASSIUM SALT	CAPSULE / ORAL	2009-03-24	`74a2ff9319b5…`
2022-03-09 01:35 UTC	2022-03	A078682-001	IBUPROFEN	EQ 200MG FREE ACID AND POTASSIUM SALT	CAPSULE / ORAL	2009-03-24	`bb7c543d1eb4…`
2021-12-28 21:50 UTC	2021-12	A078682-001	IBUPROFEN	EQ 200MG FREE ACID AND POTASSIUM SALT	CAPSULE / ORAL	2009-03-24	`782e0a99824c…`
2021-05-05 16:15 UTC · 3 captures of this ZIP	2021-05	A078682-001	IBUPROFEN	EQ 200MG FREE ACID AND POTASSIUM SALT	CAPSULE / ORAL	2009-03-24	`87673890dc5c…`
2021-03-12 10:30 UTC	2021-03	A078682-001	IBUPROFEN	EQ 200MG FREE ACID AND POTASSIUM SALT	CAPSULE / ORAL	2009-03-24	`5aa47cf7b7d7…`
2020-12-22 03:56 UTC	2020-12	A078682-001	IBUPROFEN	EQ 200MG FREE ACID AND POTASSIUM SALT	CAPSULE / ORAL	2009-03-24	`8869cabd3fbd…`
2020-11-12 02:37 UTC	2020-11	A078682-001	IBUPROFEN	EQ 200MG FREE ACID AND POTASSIUM SALT	CAPSULE / ORAL	2009-03-24	`c0c555d07b60…`
2019-12-14 00:12 UTC	2019-12	A078682-001	IBUPROFEN	EQ 200MG FREE ACID AND POTASSIUM SALT	CAPSULE / ORAL	2009-03-24	`3f01610625f2…`
2019-09-15 20:21 UTC	2019-09	A078682-001	IBUPROFEN	EQ 200MG FREE ACID AND POTASSIUM SALT	CAPSULE / ORAL	2009-03-24	`b00525d2431f…`
2019-07-19 19:46 UTC	2019-07	A078682-001	IBUPROFEN	EQ 200MG FREE ACID AND POTASSIUM SALT	CAPSULE / ORAL	2009-03-24	`ea99ee380514…`
2024-03-16 18:09 UTC · 4 captures of this ZIP	2024-03	A078682-001	IBUPROFEN	EQ 200MG FREE ACID AND POTASSIUM SALT	CAPSULE / ORAL	2009-03-24	`6a51e52b5d6a…`
2024-02-18 07:12 UTC	2024-02	A078682-001	IBUPROFEN	EQ 200MG FREE ACID AND POTASSIUM SALT	CAPSULE / ORAL	2009-03-24	`1c564ffb4f44…`
2023-12-20 04:57 UTC	2023-12	A078682-001	IBUPROFEN	EQ 200MG FREE ACID AND POTASSIUM SALT	CAPSULE / ORAL	2009-03-24	`ea1830bbd6c7…`
2023-11-28 05:40 UTC · 2 captures of this ZIP	2023-11	A078682-001	IBUPROFEN	EQ 200MG FREE ACID AND POTASSIUM SALT	CAPSULE / ORAL	2009-03-24	`a72a2bbeb626…`
2023-10-25 00:34 UTC · 2 captures of this ZIP	2023-10	A078682-001	IBUPROFEN	EQ 200MG FREE ACID AND POTASSIUM SALT	CAPSULE / ORAL	2009-03-24	`9b2671bbb829…`
2023-07-15 15:27 UTC · 2 captures of this ZIP	2023-07	A078682-001	IBUPROFEN	EQ 200MG FREE ACID AND POTASSIUM SALT	CAPSULE / ORAL	2009-03-24	`a67488948f0b…`
2023-06-13 01:57 UTC · 3 captures of this ZIP	2023-06	A078682-001	IBUPROFEN	EQ 200MG FREE ACID AND POTASSIUM SALT	CAPSULE / ORAL	2009-03-24	`3f0d92c62455…`
2023-05-13 08:27 UTC	2023-05	A078682-001	IBUPROFEN	EQ 200MG FREE ACID AND POTASSIUM SALT	CAPSULE / ORAL	2009-03-24	`053a50430f4f…`
2023-01-26 05:58 UTC	2023-01	A078682-001	IBUPROFEN	EQ 200MG FREE ACID AND POTASSIUM SALT	CAPSULE / ORAL	2009-03-24	`3bdfa0b2c4d7…`
2022-11-12 20:34 UTC · 5 captures of this ZIP	2022-11	A078682-001	IBUPROFEN	EQ 200MG FREE ACID AND POTASSIUM SALT	CAPSULE / ORAL	2009-03-24	`3a93d1ddd44b…`
2022-10-28 04:53 UTC	2022-10	A078682-001	IBUPROFEN	EQ 200MG FREE ACID AND POTASSIUM SALT	CAPSULE / ORAL	2009-03-24	`f41ea6bd6efb…`
2022-09-29 23:25 UTC	2022-09	A078682-001	IBUPROFEN	EQ 200MG FREE ACID AND POTASSIUM SALT	CAPSULE / ORAL	2009-03-24	`e64feba35796…`
2022-07-09 03:26 UTC · 3 captures of this ZIP	2022-07	A078682-001	IBUPROFEN	EQ 200MG FREE ACID AND POTASSIUM SALT	CAPSULE / ORAL	2009-03-24	`cb3db0bc1861…`

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 3 · 60 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Ibuprofen mini dye free	IBUPROFEN	CHAIN DRUG MARKETING ASSOCIATION INC.	552d9018-cc7e-7e1a-e063-6294a90a3322	2026-06-26	Warnings	Exact identifier application applno (ANDA): 078682 application number: ANDA078682
Ibuprofen	IBUPROFEN	TOP CARE (Topco Associates LLC)	fb842f4d-1228-9a52-e053-6294a90adb41	2026-06-26	Warnings	Exact identifier application applno (ANDA): 078682 application number: ANDA078682
Ibuprofen Mini Dye Free	IBUPROFEN	CVS Pharmacy	42c7dbec-2e53-70ae-e063-6294a90a16e6	2026-06-25	Warnings	Exact identifier application applno (ANDA): 078682 application number: ANDA078682
Ibuprofen	IBUPROFEN	TOP CARE (Topco Associates LLC)	c62cc12f-5a0e-389a-e053-2995a90a208c	2026-06-23	Warnings	Exact identifier application applno (ANDA): 078682 application number: ANDA078682 ndc (package): 36800-221-11 ndc (product): 36800-221 ndc11 (package): 36800022111
Ibuprofen	IBUPROFEN	TOP CARE (Topco Associates LLC)	c6297c23-3b27-c0c6-e053-2995a90a3e76	2026-06-23	Warnings	Exact identifier application applno (ANDA): 078682 application number: ANDA078682
Ibuprofen	IBUPROFEN	MEIJER DISTRIBUTION INC.	a139e495-3dbf-4998-e053-2a95a90ac136	2026-06-23	Warnings	Exact identifier application applno (ANDA): 078682 application number: ANDA078682
pain relief	IBUPROFEN	Bionpharma Inc.	a14ca126-fada-c903-e053-2995a90ae72d	2026-06-23	Warnings	Exact identifier application applno (ANDA): 078682 application number: ANDA078682
Ibuprofen	IBUPROFEN	HEB	ca4be24c-5d92-ddc9-e053-2a95a90aa5a7	2026-06-23	Warnings	Exact identifier application applno (ANDA): 078682 application number: ANDA078682
Ibuprofen	IBUPROFEN	DOLGENCORP INC	03138a6f-653a-f359-e063-6394a90ac5d6	2026-06-23	Warnings	Exact identifier application applno (ANDA): 078682 application number: ANDA078682
Ibuprofen	IBUPROFEN CAPSULE	PUBLIX SUPER MARKETS INC	10a6eba7-e400-ce97-e063-6294a90af3bd	2026-06-23	Warnings	Exact identifier application applno (ANDA): 078682 application number: ANDA078682
IBUPROFEN	IBUPROFEN	DISCOUNT DRUG MART, INC.	d07ea9e3-88b0-4aa0-903a-10555dcca37d	2026-06-23	Warnings	Exact identifier application applno (ANDA): 078682 application number: ANDA078682
Ibuprofen	IBUPROFEN	DISCOUNT DRUG MART, INC.	aae40114-343e-12da-e053-2a95a90a9213	2026-06-23	Warnings	Exact identifier application applno (ANDA): 078682 application number: ANDA078682
Ibuprofen	IBUPROFEN	BJWC	0ca0b6cf-7d1f-4673-b9b9-48f78d80c00a	2026-06-23	Warnings	Exact identifier application applno (ANDA): 078682 application number: ANDA078682
pain relief	IBUPROFEN	Bionpharma Inc.	2b4ecdd8-627a-445f-8ddc-f2b6c832c1e8	2026-06-23	Warnings	Exact identifier application applno (ANDA): 078682 application number: ANDA078682
dye-free pain relief	IBUPROFEN	Bionpharma Inc.	c46c9c36-8844-7b50-e053-2a95a90aa0e9	2026-06-23	Warnings	Exact identifier application applno (ANDA): 078682 application number: ANDA078682
dye-free pain relief	IBUPROFEN	Bionpharma Inc.	4227d0b7-846a-dcb0-e063-6294a90af7d7	2026-06-23	Warnings	Exact identifier application applno (ANDA): 078682 application number: ANDA078682
Ibuprofen	IBUPROFEN	CHAIN DRUG MARKETING ASSOCIATION INC.	3c1c1b65-f57f-62b0-e063-6294a90a1021	2026-06-23	Warnings	Exact identifier application applno (ANDA): 078682 application number: ANDA078682
Ibuprofen	IBUPROFEN	Chain Drug Marketing Association, Inc.	3802982a-2373-9ca3-e063-6394a90a0ab7	2026-06-23	Warnings	Exact identifier application applno (ANDA): 078682 application number: ANDA078682
Ibuprofen	IBUPROFEN	CHAIN DRUG MARKETING ASSOCIATION INC.	4573753d-117b-a6f2-e063-6394a90ae2f9	2026-06-23	Warnings	Exact identifier application applno (ANDA): 078682 application number: ANDA078682
Ibuprofen	IBUPROFEN	Chain Drug Marketing Association, Inc.	3ed7faff-fd48-0a83-e063-6394a90aab14	2026-06-23	Warnings	Exact identifier application applno (ANDA): 078682 application number: ANDA078682

Additional Listing Data#

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

Active Ingredients#

Ingredient, Strength table
Ingredient	Strength
IBUPROFEN	200 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 · 1 matching rows.

Identifier, FDA.report destination table
Identifier	FDA.report destination
310964	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
c62cc12f-5a0e-389a-e053-2995a90a208c	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
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

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
36800-221-11	Ibuprofen	20 in 1 BOTTLE	CAPSULE, LIQUID FILLED	20	5
36800-221-11	Ibuprofen	1 in 1 CARTON	CAPSULE, LIQUID FILLED	1	5
36800-221-78	Ibuprofen	80 in 1 BOTTLE	CAPSULE, LIQUID FILLED	80	5
36800-221-78	Ibuprofen	1 in 1 CARTON	CAPSULE, LIQUID FILLED	1	5
36800-221-79	Ibuprofen	1 in 1 CARTON	CAPSULE, LIQUID FILLED	1	5
36800-221-79	Ibuprofen	160 in 1 BOTTLE	CAPSULE, LIQUID FILLED	160	5

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
36800-221	IBUPROFEN CAPSULE, LIQUID FILLED [TOP CARE (TOPCO ASSOCIATES LLC)]	4	Current NDC, Legacy NDC, 6 package rows	20231011_c62cc12f-5a0e-389a-e053-2995a90a208c.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
310964	ibuprofen 200 MG Oral Capsule	PSN	c62cc12f-5a0e-389a-e053-2995a90a208c	5
310964	ibuprofen 200 MG Oral Capsule	SCD	c62cc12f-5a0e-389a-e053-2995a90a208c	5

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
36800-221-11	36800022111	1 BOTTLE in 1 CARTON (36800-221-11) / 20 CAPSULE, LIQUID FILLED in 1 BOTTLE	1 bottle	2021-08-18	0000-00-00	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
Drug Facts	TOP CARE (Topco Associates LLC) \| Bionpharma Inc. \| Patheon Softgels Inc. \| ESJAY PHARMA PRIVATE LIMITED	2026-06-23	HUMAN OTC DRUG LABEL	6