NuDroxiPAK I-800

Product NDC: 70859-030
11-digit product format: 708590030
Labeler code: 70859
Product ID: 70859-030_c185003e-549f-30c2-e053-2995a90af0ad
Type: HUMAN PRESCRIPTION DRUG
Nonproprietary name: Ibuprofen,Methyl Salicylate/Menthol/Capsaicin
Dosage form: KIT
Labeler: NuCare Pharmaceuticals,Inc.
Application: ANDA075682
Marketing category: ANDA
Marketing start: 2018-03-12
Marketing end: 0000-00-00
Active strength: 0
NDC exclude flag: No
Listing certified through: 2022-12-31
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 · 2 matching rows.

Dataset, Scope, Product NDC table
Dataset	Scope	Product NDC	Package NDC	Code	Status	Reporting period	Source date
excluded product	product	70859-030		D	Discontinued by firm		2026-08-03
excluded package	package	70859-030	70859-030-01	D	Discontinued by firm		2026-08-03

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 · 32 matching rows.

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

Captured / source date, Dataset, Scope table
Captured / source date	Dataset	Scope	Package NDC	Code	Status	Snapshot	Source SHA-256
2025-12-14 17:58 UTC · source 2025-12-05	excluded product	product		D	Discontinued by firm	`d630ba8d3edf…`	`732f749b63fb…`
2025-12-14 17:58 UTC · source 2025-12-05	excluded package	package	70859-030-01	D	Discontinued by firm	`d630ba8d3edf…`	`732f749b63fb…`
2025-08-27 00:01 UTC · source 2025-08-26	excluded product	product		D	Discontinued by firm	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-08-27 00:01 UTC · source 2025-08-26	excluded package	package	70859-030-01	D	Discontinued by firm	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-04-01 02:39 UTC · source 2025-03-31	excluded product	product		D	Discontinued by firm	`2ef7874e63bc…`	`57b86245f4fa…`
2025-04-01 02:39 UTC · source 2025-03-31	excluded package	package	70859-030-01	D	Discontinued by firm	`2ef7874e63bc…`	`57b86245f4fa…`
2025-03-28 20:22 UTC · source 2025-03-28	excluded product	product		D	Discontinued by firm	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-28 20:22 UTC · source 2025-03-28	excluded package	package	70859-030-01	D	Discontinued by firm	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-22 03:12 UTC · source 2025-03-21	excluded product	product		D	Discontinued by firm	`cfe11265f3b6…`	`090c488252e2…`
2025-03-22 03:12 UTC · source 2025-03-21	excluded package	package	70859-030-01	D	Discontinued by firm	`cfe11265f3b6…`	`090c488252e2…`
2025-03-10 12:48 UTC · source 2025-03-10	excluded product	product		D	Discontinued by firm	`cdf11ea48f46…`	`ba0047e9e063…`
2025-03-10 12:48 UTC · source 2025-03-10	excluded package	package	70859-030-01	D	Discontinued by firm	`cdf11ea48f46…`	`ba0047e9e063…`
2025-02-02 03:52 UTC · source 2025-01-31	excluded product	product		D	Discontinued by firm	`302b2466d912…`	`e7b80fea0513…`
2025-02-02 03:52 UTC · source 2025-01-31	excluded package	package	70859-030-01	D	Discontinued by firm	`302b2466d912…`	`e7b80fea0513…`
2025-01-20 13:05 UTC · source 2025-01-20	excluded product	product		D	Discontinued by firm	`ed331223b511…`	`672a5bd82f5f…`
2025-01-20 13:05 UTC · source 2025-01-20	excluded package	package	70859-030-01	D	Discontinued by firm	`ed331223b511…`	`672a5bd82f5f…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded product	product		D	Discontinued by firm	`0efc9e666f02…`	`f202fb6c5f17…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded package	package	70859-030-01	D	Discontinued by firm	`0efc9e666f02…`	`f202fb6c5f17…`
2024-11-09 02:27 UTC · source 2024-11-08	excluded product	product		D	Discontinued by firm	`ad56d346431e…`	`cc804d4bbf1e…`
2024-11-09 02:27 UTC · source 2024-11-08	excluded package	package	70859-030-01	D	Discontinued by firm	`ad56d346431e…`	`cc804d4bbf1e…`
2024-10-04 04:10 UTC · source 2024-10-03	excluded product	product		D	Discontinued by firm	`367a005e9d99…`	`383a685ebd0f…`
2024-10-04 04:10 UTC · source 2024-10-03	excluded package	package	70859-030-01	D	Discontinued by firm	`367a005e9d99…`	`383a685ebd0f…`
2024-05-28 21:12 UTC · source 2024-05-28	excluded product	product		I	Inactivated by FDA	`8af77b9d5b6f…`	`d9bbb34c5368…`
2024-05-28 21:12 UTC · source 2024-05-28	excluded package	package	70859-030-01	I	Inactivated by FDA	`8af77b9d5b6f…`	`d9bbb34c5368…`
2024-05-15 03:39 UTC · source 2024-05-14	excluded product	product		I	Inactivated by FDA	`834df4deac94…`	`adcc014656a3…`
2024-05-15 03:39 UTC · source 2024-05-14	excluded package	package	70859-030-01	I	Inactivated by FDA	`834df4deac94…`	`adcc014656a3…`
2024-03-11 06:39 UTC · source 2024-03-08	excluded product	product		I	Inactivated by FDA	`1332a3947898…`	`d4bfe170f9cd…`
2024-03-11 06:39 UTC · source 2024-03-08	excluded package	package	70859-030-01	I	Inactivated by FDA	`1332a3947898…`	`d4bfe170f9cd…`
2020-12-18 03:04 UTC · source 2020-12-17	excluded product	product		I	Inactivated by FDA	`e2bbac7714bc…`	`27bdfed8d636…`
2020-12-18 03:04 UTC · source 2020-12-17	excluded package	package	70859-030-01	I	Inactivated by FDA	`e2bbac7714bc…`	`27bdfed8d636…`
2020-06-10 20:45 UTC · source 2020-06-10	excluded product	product		I	Inactivated by FDA	`9bebd1f3094a…`	`5416666fcb17…`
2020-06-10 20:45 UTC · source 2020-06-10	excluded package	package	70859-030-01	I	Inactivated by FDA	`9bebd1f3094a…`	`5416666fcb17…`

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	RLD / RS	Approval date
A075682-001	IBUPROFEN	IBUPROFEN	400MG	TABLET / ORAL	AB		2001-11-14
A075682-002	IBUPROFEN	IBUPROFEN	600MG	TABLET / ORAL	AB		2001-11-14
A075682-003	IBUPROFEN	IBUPROFEN	800MG	TABLET / ORAL	AB	RS	2001-11-14

Therapeutic equivalence codes#

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

Application-product, TE code table
Application-product	TE code
A075682-001	AB
A075682-002	AB
A075682-003	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.

Product history page 1 of 4 · 123 observed states.

Captured, Edition, Application-product table
Captured	Edition	Application-product	Trade name	Strength	Dosage form / route	Product TE source text	RLD / RS	Approval date	Source SHA-256
2026-02-19 14:30 UTC	2026-02	A075682-001	IBUPROFEN	400MG	TABLET / ORAL	AB		2001-11-14	`011fe1cb6892…`
2026-02-19 14:30 UTC	2026-02	A075682-002	IBUPROFEN	600MG	TABLET / ORAL	AB		2001-11-14	`011fe1cb6892…`
2026-02-19 14:30 UTC	2026-02	A075682-003	IBUPROFEN	800MG	TABLET / ORAL	AB	RS	2001-11-14	`011fe1cb6892…`
2025-12-14 10:44 UTC · 2 captures of this ZIP	2025-12	A075682-001	IBUPROFEN	400MG	TABLET / ORAL	AB		2001-11-14	`31067a03dcf5…`
2025-12-14 10:44 UTC · 2 captures of this ZIP	2025-12	A075682-002	IBUPROFEN	600MG	TABLET / ORAL	AB		2001-11-14	`31067a03dcf5…`
2025-12-14 10:44 UTC · 2 captures of this ZIP	2025-12	A075682-003	IBUPROFEN	800MG	TABLET / ORAL	AB	RS	2001-11-14	`31067a03dcf5…`
2025-08-23 18:47 UTC	2025-08	A075682-001	IBUPROFEN	400MG	TABLET / ORAL	AB		2001-11-14	`6a471c1ec25d…`
2025-08-23 18:47 UTC	2025-08	A075682-002	IBUPROFEN	600MG	TABLET / ORAL	AB		2001-11-14	`6a471c1ec25d…`
2025-08-23 18:47 UTC	2025-08	A075682-003	IBUPROFEN	800MG	TABLET / ORAL	AB	RS	2001-11-14	`6a471c1ec25d…`
2025-03-22 03:13 UTC · 3 captures of this ZIP	2025-03	A075682-001	IBUPROFEN	400MG	TABLET / ORAL	AB		2001-11-14	`fd3edfee7708…`
2025-03-22 03:13 UTC · 3 captures of this ZIP	2025-03	A075682-002	IBUPROFEN	600MG	TABLET / ORAL	AB		2001-11-14	`fd3edfee7708…`
2025-03-22 03:13 UTC · 3 captures of this ZIP	2025-03	A075682-003	IBUPROFEN	800MG	TABLET / ORAL	AB	RS	2001-11-14	`fd3edfee7708…`
2025-02-26 10:13 UTC · 3 captures of this ZIP	2025-02	A075682-001	IBUPROFEN	400MG	TABLET / ORAL	AB		2001-11-14	`b8a1b40f171c…`
2025-02-26 10:13 UTC · 3 captures of this ZIP	2025-02	A075682-002	IBUPROFEN	600MG	TABLET / ORAL	AB		2001-11-14	`b8a1b40f171c…`
2025-02-26 10:13 UTC · 3 captures of this ZIP	2025-02	A075682-003	IBUPROFEN	800MG	TABLET / ORAL	AB	RS	2001-11-14	`b8a1b40f171c…`
2025-01-19 17:59 UTC · 7 captures of this ZIP	2025-01	A075682-001	IBUPROFEN	400MG	TABLET / ORAL	AB		2001-11-14	`03ed91905a0d…`
2025-01-19 17:59 UTC · 7 captures of this ZIP	2025-01	A075682-002	IBUPROFEN	600MG	TABLET / ORAL	AB		2001-11-14	`03ed91905a0d…`
2025-01-19 17:59 UTC · 7 captures of this ZIP	2025-01	A075682-003	IBUPROFEN	800MG	TABLET / ORAL	AB	RS	2001-11-14	`03ed91905a0d…`
2024-12-13 21:23 UTC · 2 captures of this ZIP	2024-12	A075682-001	IBUPROFEN	400MG	TABLET / ORAL	AB		2001-11-14	`2680178bc6a6…`
2024-12-13 21:23 UTC · 2 captures of this ZIP	2024-12	A075682-002	IBUPROFEN	600MG	TABLET / ORAL	AB		2001-11-14	`2680178bc6a6…`
2024-12-13 21:23 UTC · 2 captures of this ZIP	2024-12	A075682-003	IBUPROFEN	800MG	TABLET / ORAL	AB	RS	2001-11-14	`2680178bc6a6…`
2024-09-14 05:58 UTC · 2 captures of this ZIP	2024-09	A075682-001	IBUPROFEN	400MG	TABLET / ORAL	AB		2001-11-14	`5bbf6a4d5a75…`
2024-09-14 05:58 UTC · 2 captures of this ZIP	2024-09	A075682-002	IBUPROFEN	600MG	TABLET / ORAL	AB		2001-11-14	`5bbf6a4d5a75…`
2024-09-14 05:58 UTC · 2 captures of this ZIP	2024-09	A075682-003	IBUPROFEN	800MG	TABLET / ORAL	AB	RS	2001-11-14	`5bbf6a4d5a75…`
2024-11-08 22:44 UTC · 3 captures of this ZIP	2024-11	A075682-001	IBUPROFEN	400MG	TABLET / ORAL	AB		2001-11-14	`d8e5a09893c0…`
2024-11-08 22:44 UTC · 3 captures of this ZIP	2024-11	A075682-002	IBUPROFEN	600MG	TABLET / ORAL	AB		2001-11-14	`d8e5a09893c0…`
2024-11-08 22:44 UTC · 3 captures of this ZIP	2024-11	A075682-003	IBUPROFEN	800MG	TABLET / ORAL	AB	RS	2001-11-14	`d8e5a09893c0…`
2024-10-29 15:01 UTC	2024-10	A075682-001	IBUPROFEN	400MG	TABLET / ORAL	AB		2001-11-14	`d06236e962d9…`
2024-10-29 15:01 UTC	2024-10	A075682-002	IBUPROFEN	600MG	TABLET / ORAL	AB		2001-11-14	`d06236e962d9…`
2024-10-29 15:01 UTC	2024-10	A075682-003	IBUPROFEN	800MG	TABLET / ORAL	AB	RS	2001-11-14	`d06236e962d9…`
2024-08-13 05:28 UTC · 3 captures of this ZIP	2024-08	A075682-001	IBUPROFEN	400MG	TABLET / ORAL	AB		2001-11-14	`79d66fd596c7…`
2024-08-13 05:28 UTC · 3 captures of this ZIP	2024-08	A075682-002	IBUPROFEN	600MG	TABLET / ORAL	AB		2001-11-14	`79d66fd596c7…`
2024-08-13 05:28 UTC · 3 captures of this ZIP	2024-08	A075682-003	IBUPROFEN	800MG	TABLET / ORAL	AB	RS	2001-11-14	`79d66fd596c7…`
2024-07-13 05:37 UTC · 2 captures of this ZIP	2024-07	A075682-001	IBUPROFEN	400MG	TABLET / ORAL	AB		2001-11-14	`301d65b070ca…`
2024-07-13 05:37 UTC · 2 captures of this ZIP	2024-07	A075682-002	IBUPROFEN	600MG	TABLET / ORAL	AB		2001-11-14	`301d65b070ca…`
2024-07-13 05:37 UTC · 2 captures of this ZIP	2024-07	A075682-003	IBUPROFEN	800MG	TABLET / ORAL	AB	RS	2001-11-14	`301d65b070ca…`
2024-06-18 03:08 UTC · 5 captures of this ZIP	2024-06	A075682-001	IBUPROFEN	400MG	TABLET / ORAL	AB		2001-11-14	`1e350fbaab3a…`
2024-06-18 03:08 UTC · 5 captures of this ZIP	2024-06	A075682-002	IBUPROFEN	600MG	TABLET / ORAL	AB		2001-11-14	`1e350fbaab3a…`
2024-06-18 03:08 UTC · 5 captures of this ZIP	2024-06	A075682-003	IBUPROFEN	800MG	TABLET / ORAL	AB	RS	2001-11-14	`1e350fbaab3a…`
2024-05-31 18:47 UTC	2024-05	A075682-001	IBUPROFEN	400MG	TABLET / ORAL	AB		2001-11-14	`8072bd15b7f6…`

Observed Orange Book normalized TE history#

Normalized TE history page 1 of 4 · 123 observed states.

Captured, Edition, Application-product table
Captured	Edition	Application-product	TE code	Order	Source SHA-256
2026-02-19 14:30 UTC	2026-02	A075682-001	AB	1	`011fe1cb6892…`
2026-02-19 14:30 UTC	2026-02	A075682-002	AB	1	`011fe1cb6892…`
2026-02-19 14:30 UTC	2026-02	A075682-003	AB	1	`011fe1cb6892…`
2025-12-14 10:44 UTC · 2 captures of this ZIP	2025-12	A075682-001	AB	1	`31067a03dcf5…`
2025-12-14 10:44 UTC · 2 captures of this ZIP	2025-12	A075682-002	AB	1	`31067a03dcf5…`
2025-12-14 10:44 UTC · 2 captures of this ZIP	2025-12	A075682-003	AB	1	`31067a03dcf5…`
2025-08-23 18:47 UTC	2025-08	A075682-001	AB	1	`6a471c1ec25d…`
2025-08-23 18:47 UTC	2025-08	A075682-002	AB	1	`6a471c1ec25d…`
2025-08-23 18:47 UTC	2025-08	A075682-003	AB	1	`6a471c1ec25d…`
2025-03-22 03:13 UTC · 3 captures of this ZIP	2025-03	A075682-001	AB	1	`fd3edfee7708…`
2025-03-22 03:13 UTC · 3 captures of this ZIP	2025-03	A075682-002	AB	1	`fd3edfee7708…`
2025-03-22 03:13 UTC · 3 captures of this ZIP	2025-03	A075682-003	AB	1	`fd3edfee7708…`
2025-02-26 10:13 UTC · 3 captures of this ZIP	2025-02	A075682-001	AB	1	`b8a1b40f171c…`
2025-02-26 10:13 UTC · 3 captures of this ZIP	2025-02	A075682-002	AB	1	`b8a1b40f171c…`
2025-02-26 10:13 UTC · 3 captures of this ZIP	2025-02	A075682-003	AB	1	`b8a1b40f171c…`
2025-01-19 17:59 UTC · 7 captures of this ZIP	2025-01	A075682-001	AB	1	`03ed91905a0d…`
2025-01-19 17:59 UTC · 7 captures of this ZIP	2025-01	A075682-002	AB	1	`03ed91905a0d…`
2025-01-19 17:59 UTC · 7 captures of this ZIP	2025-01	A075682-003	AB	1	`03ed91905a0d…`
2024-12-13 21:23 UTC · 2 captures of this ZIP	2024-12	A075682-001	AB	1	`2680178bc6a6…`
2024-12-13 21:23 UTC · 2 captures of this ZIP	2024-12	A075682-002	AB	1	`2680178bc6a6…`
2024-12-13 21:23 UTC · 2 captures of this ZIP	2024-12	A075682-003	AB	1	`2680178bc6a6…`
2024-09-14 05:58 UTC · 2 captures of this ZIP	2024-09	A075682-001	AB	1	`5bbf6a4d5a75…`
2024-09-14 05:58 UTC · 2 captures of this ZIP	2024-09	A075682-002	AB	1	`5bbf6a4d5a75…`
2024-09-14 05:58 UTC · 2 captures of this ZIP	2024-09	A075682-003	AB	1	`5bbf6a4d5a75…`
2024-11-08 22:44 UTC · 3 captures of this ZIP	2024-11	A075682-001	AB	1	`d8e5a09893c0…`
2024-11-08 22:44 UTC · 3 captures of this ZIP	2024-11	A075682-002	AB	1	`d8e5a09893c0…`
2024-11-08 22:44 UTC · 3 captures of this ZIP	2024-11	A075682-003	AB	1	`d8e5a09893c0…`
2024-10-29 15:01 UTC	2024-10	A075682-001	AB	1	`d06236e962d9…`
2024-10-29 15:01 UTC	2024-10	A075682-002	AB	1	`d06236e962d9…`
2024-10-29 15:01 UTC	2024-10	A075682-003	AB	1	`d06236e962d9…`
2024-08-13 05:28 UTC · 3 captures of this ZIP	2024-08	A075682-001	AB	1	`79d66fd596c7…`
2024-08-13 05:28 UTC · 3 captures of this ZIP	2024-08	A075682-002	AB	1	`79d66fd596c7…`
2024-08-13 05:28 UTC · 3 captures of this ZIP	2024-08	A075682-003	AB	1	`79d66fd596c7…`
2024-07-13 05:37 UTC · 2 captures of this ZIP	2024-07	A075682-001	AB	1	`301d65b070ca…`
2024-07-13 05:37 UTC · 2 captures of this ZIP	2024-07	A075682-002	AB	1	`301d65b070ca…`
2024-07-13 05:37 UTC · 2 captures of this ZIP	2024-07	A075682-003	AB	1	`301d65b070ca…`
2024-06-18 03:08 UTC · 5 captures of this ZIP	2024-06	A075682-001	AB	1	`1e350fbaab3a…`
2024-06-18 03:08 UTC · 5 captures of this ZIP	2024-06	A075682-002	AB	1	`1e350fbaab3a…`
2024-06-18 03:08 UTC · 5 captures of this ZIP	2024-06	A075682-003	AB	1	`1e350fbaab3a…`
2024-05-31 18:47 UTC	2024-05	A075682-001	AB	1	`8072bd15b7f6…`

FDA-Initiated Inactive NDC Indexing#

Effective, Related label table
Effective	Related label
2024-06-11	NuDroxIPAK I-800 pain relief PAK These highlights do not include all the information needed to use Meloxicam Tablets USP. safely and effectively. See full prescribing information for Meloxicam Tablets USP. Meloxicam Tablets USP, for oral use Initial U.S. Approval: 2000
2023-01-30	NuDroxIPAK I-800 pain relief PAK These highlights do not include all the information needed to use Meloxicam Tablets USP. safely and effectively. See full prescribing information for Meloxicam Tablets USP. Meloxicam Tablets USP, for oral use Initial U.S. Approval: 2000
2021-05-04	NuDroxIPAK I-800 pain relief PAK These highlights do not include all the information needed to use Meloxicam Tablets USP. safely and effectively. See full prescribing information for Meloxicam Tablets USP. Meloxicam Tablets USP, for oral use Initial U.S. Approval: 2000
2020-01-31	NuDroxIPAK I-800 pain relief PAK These highlights do not include all the information needed to use Meloxicam Tablets USP. safely and effectively. See full prescribing information for Meloxicam Tablets USP. Meloxicam Tablets USP, for oral use Initial U.S. Approval: 2000

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
70859-030-01	EA - Each	70859-030	1ada4d42-bcca-490b-8b1b-14db70b9f60e	1	2018-05-09

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 · 21 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Ibuprofen	IBUPROFEN	Preferred Pharmaceuticals, Inc.	72ec2491-924d-460f-9510-62d624d54b59	2026-05-13	Boxed warning, Warnings, Adverse reactions	Exact identifier application applno (ANDA): 075682 application number: ANDA075682
IBU	IBUPROFEN	Golden State Medical Supply, Inc.	bbf4821d-f9fc-9f6e-e053-2a95a90a5253	2026-04-14	Boxed warning, Warnings, Adverse reactions	Exact identifier application applno (ANDA): 075682 application number: ANDA075682
Ibuprofen	IBUPROFEN	Aphena Pharma Solutions - Tennessee, LLC	4522b794-5c93-44cd-e063-6394a90ab39a	2026-02-20	Boxed warning, Warnings, Adverse reactions	Exact identifier application applno (ANDA): 075682 application number: ANDA075682
Ibuprofen	IBUPROFEN	Aphena Pharma Solutions - Tennessee, LLC	45223597-0ea8-b275-e063-6394a90a8412	2025-12-04	Boxed warning, Warnings, Adverse reactions	Exact identifier application applno (ANDA): 075682 application number: ANDA075682
Ibuprofen	IBUPROFEN	Aphena Pharma Solutions - Tennessee, LLC	4522cb9e-4999-c455-e063-6294a90a294f	2025-12-04	Boxed warning, Warnings, Adverse reactions	Exact identifier application applno (ANDA): 075682 application number: ANDA075682
IBU	IBUPROFEN	Proficient Rx LP	a7098fa1-b5ae-485e-ada9-64154f81fb6a	2025-12-01	Boxed warning, Warnings, Adverse reactions	Exact identifier application applno (ANDA): 075682 application number: ANDA075682
Ibuprofen	IBUPROFEN	Golden State Medical Supply, Inc.	3ff501eb-5ae3-8824-e063-6394a90ac58e	2025-11-19	Boxed warning, Warnings, Adverse reactions	Exact identifier application applno (ANDA): 075682 application number: ANDA075682
Ibuprofen	IBUPROFEN	Major Pharmaceuticals	ba86e936-ef72-43e5-aebf-f2c788fe2266	2025-09-19	Boxed warning, Warnings, Adverse reactions	Exact identifier application applno (ANDA): 075682 application number: ANDA075682
Ibuprofen	IBUPROFEN	Cardinal Health 107, LLC	8ea0e303-3967-4d71-8255-ac42a841ce28	2025-08-08	Boxed warning, Warnings, Adverse reactions	Exact identifier application applno (ANDA): 075682 application number: ANDA075682
IBU	IBUPROFEN	Dr. Reddy's Laboratories Limited	24731405-219c-79b4-ecf0-7d5fbfda94ba	2025-07-02	Boxed warning, Warnings, Adverse reactions	Exact identifier application applno (ANDA): 075682 application number: ANDA075682
IBU	IBU	RedPharm Drug, Inc.	4db219dc-ea48-490c-e054-00144ff88e88	2025-04-09	Boxed warning, Warnings, Adverse reactions	Exact identifier application applno (ANDA): 075682 application number: ANDA075682
Ibuprofen	IBUPROFEN	Aphena Pharma Solutions - Tennessee, LLC	31e6005b-492e-7936-e063-6394a90ad801	2025-04-03	Boxed warning, Warnings, Adverse reactions	Exact identifier application applno (ANDA): 075682 application number: ANDA075682
Ibuprofen	IBUPROFEN	Aphena Pharma Solutions - Tennessee, LLC	31e6ac7a-fa3e-4dd4-e063-6294a90a29af	2025-04-03	Boxed warning, Warnings, Adverse reactions	Exact identifier application applno (ANDA): 075682 application number: ANDA075682
Ibuprofen	IBUPROFEN	Bryant Ranch Prepack	7650f84b-92f2-4065-8ef2-f5de5bd7002b	2024-10-29	Boxed warning, Warnings, Adverse reactions	Exact identifier application applno (ANDA): 075682 application number: ANDA075682
IBU	IBUPROFEN	NuCare Pharmaceuticals,Inc.	593d9870-0213-75e6-e053-2991aa0a0eff	2024-08-14	Boxed warning, Warnings, Adverse reactions	Exact identifier application applno (ANDA): 075682 application number: ANDA075682
IBU	IBUPROFEN	NuCare Pharmaceuticals Inc.	575c275c-3e1a-0572-e053-2991aa0adabd	2024-08-14	Boxed warning, Warnings, Adverse reactions	Exact identifier application applno (ANDA): 075682 application number: ANDA075682
IBU	IBUPROFEN	NuCare Pharmaceuticals,Inc.	678e2d16-33f3-67a7-e053-2991aa0a1132	2024-07-18	Boxed warning, Warnings, Adverse reactions	Exact identifier application applno (ANDA): 075682 application number: ANDA075682
IBU	IBUPROFEN	Proficient Rx LP	ea6f626d-cda3-46e2-9ac9-4e72204cb726	2023-03-01	Boxed warning, Warnings, Adverse reactions	Exact identifier application applno (ANDA): 075682 application number: ANDA075682
IBU	IBUPROFEN	Aphena Pharma Solutions - Tennessee, LLC	b0f03994-b744-4d66-95b7-8c86217882bc	2021-05-24	Boxed warning, Warnings, Adverse reactions	Exact identifier application applno (ANDA): 075682 application number: ANDA075682
IBU	IBUPROFEN	Aphena Pharma Solutions - Tennessee, LLC	3e45f971-b6f7-4ec5-9d8e-1b9127b6c0bd	2021-01-21	Boxed warning, Warnings, Adverse reactions	Exact identifier application applno (ANDA): 075682 application number: ANDA075682

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
70859-030-01	70859003001	1 KIT in 1 CARTON (70859-030-01) * 1 CONTAINER in 1 CARTON (70859-028-03) > 90 mL in 1 CONTAINER * 100 TABLET in 1 BOTTLE (55111-684-01)	1 kit	2018-03-12	0000-00-00	No	No	Current