Pain and Fever Relief

Product NDC: 72090-003
11-digit product format: 720900003
Labeler code: 72090
Product ID: 72090-003_c29fe377-2308-9b47-e053-2995a90a3846
Type: HUMAN OTC DRUG
Nonproprietary name: Naproxen Sodium
Dosage form: TABLET
Route: ORAL
Labeler: Pioneer Life Sciences, LLC
Application: ANDA207612
Marketing category: ANDA
Marketing start: 2021-05-19
Marketing end: 0000-00-00
Substance: NAPROXEN SODIUM
Active strength: 220 mg/1
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	72090-003		I	Inactivated by FDA		2026-08-10
excluded package	package	72090-003	72090-003-01	I	Inactivated by FDA		2026-08-10

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 · 30 matching rows.

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

Captured / source date, Dataset, Scope table
Captured / source date	Dataset	Scope	Package NDC	Snapshot	Source SHA-256
2025-12-14 17:58 UTC · source 2025-12-05	excluded product	product		`d630ba8d3edf…`	`732f749b63fb…`
2025-12-14 17:58 UTC · source 2025-12-05	excluded package	package	72090-003-01	`d630ba8d3edf…`	`732f749b63fb…`
2025-08-27 00:01 UTC · source 2025-08-26	excluded product	product		`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-08-27 00:01 UTC · source 2025-08-26	excluded package	package	72090-003-01	`f5e01cc5f278…`	`a2eaf40c39c3…`
2025-04-01 02:39 UTC · source 2025-03-31	excluded product	product		`2ef7874e63bc…`	`57b86245f4fa…`
2025-04-01 02:39 UTC · source 2025-03-31	excluded package	package	72090-003-01	`2ef7874e63bc…`	`57b86245f4fa…`
2025-03-28 20:22 UTC · source 2025-03-28	excluded product	product		`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-28 20:22 UTC · source 2025-03-28	excluded package	package	72090-003-01	`a1b67e2a42f9…`	`c4cf2c586c0d…`
2025-03-22 03:12 UTC · source 2025-03-21	excluded product	product		`cfe11265f3b6…`	`090c488252e2…`
2025-03-22 03:12 UTC · source 2025-03-21	excluded package	package	72090-003-01	`cfe11265f3b6…`	`090c488252e2…`
2025-03-10 12:48 UTC · source 2025-03-10	excluded product	product		`cdf11ea48f46…`	`ba0047e9e063…`
2025-03-10 12:48 UTC · source 2025-03-10	excluded package	package	72090-003-01	`cdf11ea48f46…`	`ba0047e9e063…`
2025-02-02 03:52 UTC · source 2025-01-31	excluded product	product		`302b2466d912…`	`e7b80fea0513…`
2025-02-02 03:52 UTC · source 2025-01-31	excluded package	package	72090-003-01	`302b2466d912…`	`e7b80fea0513…`
2025-01-20 13:05 UTC · source 2025-01-20	excluded product	product		`ed331223b511…`	`672a5bd82f5f…`
2025-01-20 13:05 UTC · source 2025-01-20	excluded package	package	72090-003-01	`ed331223b511…`	`672a5bd82f5f…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded product	product		`0efc9e666f02…`	`f202fb6c5f17…`
2025-01-11 03:41 UTC · source 2025-01-10	excluded package	package	72090-003-01	`0efc9e666f02…`	`f202fb6c5f17…`
2024-11-09 02:27 UTC · source 2024-11-08	excluded product	product		`ad56d346431e…`	`cc804d4bbf1e…`
2024-11-09 02:27 UTC · source 2024-11-08	excluded package	package	72090-003-01	`ad56d346431e…`	`cc804d4bbf1e…`
2024-10-04 04:10 UTC · source 2024-10-03	excluded product	product		`367a005e9d99…`	`383a685ebd0f…`
2024-10-04 04:10 UTC · source 2024-10-03	excluded package	package	72090-003-01	`367a005e9d99…`	`383a685ebd0f…`
2024-07-10 04:00 UTC · source 2024-07-09	excluded product	product		`557ba5c1ecfa…`	`9c80585c8c6e…`
2024-07-10 04:00 UTC · source 2024-07-09	excluded package	package	72090-003-01	`557ba5c1ecfa…`	`9c80585c8c6e…`
2024-05-28 21:12 UTC · source 2024-05-28	excluded product	product		`8af77b9d5b6f…`	`d9bbb34c5368…`
2024-05-28 21:12 UTC · source 2024-05-28	excluded package	package	72090-003-01	`8af77b9d5b6f…`	`d9bbb34c5368…`
2024-05-15 03:39 UTC · source 2024-05-14	excluded product	product		`834df4deac94…`	`adcc014656a3…`
2024-05-15 03:39 UTC · source 2024-05-14	excluded package	package	72090-003-01	`834df4deac94…`	`adcc014656a3…`
2024-03-11 06:39 UTC · source 2024-03-08	excluded product	product		`1332a3947898…`	`d4bfe170f9cd…`
2024-03-11 06:39 UTC · source 2024-03-08	excluded package	package	72090-003-01	`1332a3947898…`	`d4bfe170f9cd…`

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
A207612-001	NAPROXEN SODIUM	NAPROXEN SODIUM	220MG	TABLET / ORAL			2018-11-16

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	A207612-001	NAPROXEN SODIUM	220MG	TABLET / ORAL	2018-11-16	`011fe1cb6892…`
2025-12-14 10:44 UTC · 2 captures of this ZIP	2025-12	A207612-001	NAPROXEN SODIUM	220MG	TABLET / ORAL	2018-11-16	`31067a03dcf5…`
2025-08-23 18:47 UTC	2025-08	A207612-001	NAPROXEN SODIUM	220MG	TABLET / ORAL	2018-11-16	`6a471c1ec25d…`
2025-03-22 03:13 UTC · 3 captures of this ZIP	2025-03	A207612-001	NAPROXEN SODIUM	220MG	TABLET / ORAL	2018-11-16	`fd3edfee7708…`
2025-02-26 10:13 UTC · 3 captures of this ZIP	2025-02	A207612-001	NAPROXEN SODIUM	220MG	TABLET / ORAL	2018-11-16	`b8a1b40f171c…`
2025-01-19 17:59 UTC · 7 captures of this ZIP	2025-01	A207612-001	NAPROXEN SODIUM	220MG	TABLET / ORAL	2018-11-16	`03ed91905a0d…`
2024-12-13 21:23 UTC · 2 captures of this ZIP	2024-12	A207612-001	NAPROXEN SODIUM	220MG	TABLET / ORAL	2018-11-16	`2680178bc6a6…`
2024-09-14 05:58 UTC · 2 captures of this ZIP	2024-09	A207612-001	NAPROXEN SODIUM	220MG	TABLET / ORAL	2018-11-16	`5bbf6a4d5a75…`
2024-11-08 22:44 UTC · 3 captures of this ZIP	2024-11	A207612-001	NAPROXEN SODIUM	220MG	TABLET / ORAL	2018-11-16	`d8e5a09893c0…`
2024-10-29 15:01 UTC	2024-10	A207612-001	NAPROXEN SODIUM	220MG	TABLET / ORAL	2018-11-16	`d06236e962d9…`
2024-08-13 05:28 UTC · 3 captures of this ZIP	2024-08	A207612-001	NAPROXEN SODIUM	220MG	TABLET / ORAL	2018-11-16	`79d66fd596c7…`
2024-07-13 05:37 UTC · 2 captures of this ZIP	2024-07	A207612-001	NAPROXEN SODIUM	220MG	TABLET / ORAL	2018-11-16	`301d65b070ca…`
2024-06-18 03:08 UTC · 5 captures of this ZIP	2024-06	A207612-001	NAPROXEN SODIUM	220MG	TABLET / ORAL	2018-11-16	`1e350fbaab3a…`
2024-05-31 18:47 UTC	2024-05	A207612-001	NAPROXEN SODIUM	220MG	TABLET / ORAL	2018-11-16	`8072bd15b7f6…`
2022-06-29 02:47 UTC · 2 captures of this ZIP	2022-06	A207612-001	NAPROXEN SODIUM	220MG	TABLET / ORAL	2018-11-16	`5c6f7cd8ea54…`
2022-04-08 23:34 UTC	2022-04	A207612-001	NAPROXEN SODIUM	220MG	TABLET / ORAL	2018-11-16	`5d02ea3f76ae…`
2022-04-04 05:41 UTC	2022-04	A207612-001	NAPROXEN SODIUM	220MG	TABLET / ORAL	2018-11-16	`4b0b4de00fa7…`
2019-12-13 00:20 UTC	2019-12	A207612-001	NAPROXEN SODIUM	220MG	TABLET / ORAL	2018-11-16	`74a2ff9319b5…`
2022-03-09 01:35 UTC	2022-03	A207612-001	NAPROXEN SODIUM	220MG	TABLET / ORAL	2018-11-16	`bb7c543d1eb4…`
2021-12-28 21:50 UTC	2021-12	A207612-001	NAPROXEN SODIUM	220MG	TABLET / ORAL	2018-11-16	`782e0a99824c…`
2021-05-05 16:15 UTC · 3 captures of this ZIP	2021-05	A207612-001	NAPROXEN SODIUM	220MG	TABLET / ORAL	2018-11-16	`87673890dc5c…`
2021-03-12 10:30 UTC	2021-03	A207612-001	NAPROXEN SODIUM	220MG	TABLET / ORAL	2018-11-16	`5aa47cf7b7d7…`
2020-12-22 03:56 UTC	2020-12	A207612-001	NAPROXEN SODIUM	220MG	TABLET / ORAL	2018-11-16	`8869cabd3fbd…`
2020-11-12 02:37 UTC	2020-11	A207612-001	NAPROXEN SODIUM	220MG	TABLET / ORAL	2018-11-16	`c0c555d07b60…`
2019-12-14 00:12 UTC	2019-12	A207612-001	NAPROXEN SODIUM	220MG	TABLET / ORAL	2018-11-16	`3f01610625f2…`
2019-09-15 20:21 UTC	2019-09	A207612-001	NAPROXEN SODIUM	EQ 200MG BASE	TABLET / ORAL	2018-11-16	`b00525d2431f…`
2019-07-19 19:46 UTC	2019-07	A207612-001	NAPROXEN SODIUM	EQ 200MG BASE	TABLET / ORAL	2018-11-16	`ea99ee380514…`
2024-03-16 18:09 UTC · 4 captures of this ZIP	2024-03	A207612-001	NAPROXEN SODIUM	220MG	TABLET / ORAL	2018-11-16	`6a51e52b5d6a…`
2024-02-18 07:12 UTC	2024-02	A207612-001	NAPROXEN SODIUM	220MG	TABLET / ORAL	2018-11-16	`1c564ffb4f44…`
2023-12-20 04:57 UTC	2023-12	A207612-001	NAPROXEN SODIUM	220MG	TABLET / ORAL	2018-11-16	`ea1830bbd6c7…`
2023-11-28 05:40 UTC · 2 captures of this ZIP	2023-11	A207612-001	NAPROXEN SODIUM	220MG	TABLET / ORAL	2018-11-16	`a72a2bbeb626…`
2023-10-25 00:34 UTC · 2 captures of this ZIP	2023-10	A207612-001	NAPROXEN SODIUM	220MG	TABLET / ORAL	2018-11-16	`9b2671bbb829…`
2023-07-15 15:27 UTC · 2 captures of this ZIP	2023-07	A207612-001	NAPROXEN SODIUM	220MG	TABLET / ORAL	2018-11-16	`a67488948f0b…`
2023-06-13 01:57 UTC · 3 captures of this ZIP	2023-06	A207612-001	NAPROXEN SODIUM	220MG	TABLET / ORAL	2018-11-16	`3f0d92c62455…`
2023-05-13 08:27 UTC	2023-05	A207612-001	NAPROXEN SODIUM	220MG	TABLET / ORAL	2018-11-16	`053a50430f4f…`
2023-01-26 05:58 UTC	2023-01	A207612-001	NAPROXEN SODIUM	220MG	TABLET / ORAL	2018-11-16	`3bdfa0b2c4d7…`
2022-11-12 20:34 UTC · 5 captures of this ZIP	2022-11	A207612-001	NAPROXEN SODIUM	220MG	TABLET / ORAL	2018-11-16	`3a93d1ddd44b…`
2022-10-28 04:53 UTC	2022-10	A207612-001	NAPROXEN SODIUM	220MG	TABLET / ORAL	2018-11-16	`f41ea6bd6efb…`
2022-09-29 23:25 UTC	2022-09	A207612-001	NAPROXEN SODIUM	220MG	TABLET / ORAL	2018-11-16	`e64feba35796…`
2022-07-09 03:26 UTC · 3 captures of this ZIP	2022-07	A207612-001	NAPROXEN SODIUM	220MG	TABLET / ORAL	2018-11-16	`cb3db0bc1861…`

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
fef6ad89-235f-4274-ba49-a8e53642473e	Product name	2	20250225
87fed3e6-8fba-48ef-96b0-3a7fb54b96ff	Product name	3	20230306
b5fdaaec-7251-4da6-9cb2-4e9e76939ec8	Product name	1	20200623
e76dbbc1-775d-722c-08ff-ed45e8a80def	Product name	3	20181002
6f4f4521-fd56-1ae6-888b-3b021bd75c7c	Product name	1	20140508
ce67e27d-1d21-5465-4409-b0662dd99d4d	Product name	1	20140508

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
72090-003-01	2023-01-30	C162847	48780-1	f386c649-e604-0266-e053-dadaa90a7c1a	c29fec0c-a858-ef95-e053-2995a90a81d8

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	Strength	SPL version
72090-003-01	Pain and Fever Relief	300 in 1 BOTTLE	TABLET	300		1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
72090-003	PAIN AND FEVER RELIEF (NAPROXEN SODIUM) TABLET [PIONEER LIFE SCIENCES, LLC]	1	Legacy NDC, 1 package rows	20210520_c29fec0c-a858-ef95-e053-2995a90a81d8.zip

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
9TN87S3A3C	NAPROXEN SODIUM	26159-34-2	NAPROXEN SODIUM

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
849574	naproxen sodium 220 MG Oral Tablet	PSN	c29fec0c-a858-ef95-e053-2995a90a81d8	1
849574	naproxen sodium 220 MG Oral Tablet	SCD	c29fec0c-a858-ef95-e053-2995a90a81d8	1
849574	naproxen sodium 220 MG (as naproxen 200 MG) Oral Tablet	SY	c29fec0c-a858-ef95-e053-2995a90a81d8	1

Packages#

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Units	Marketing start	Marketing end	Sample	Exclude flag	Status
72090-003-01	72090000301	300 TABLET in 1 BOTTLE (72090-003-01)	300 tablet	2021-05-19	0000-00-00	No	No	Current

Title, Manufacturer, Effective date table
Title	Manufacturer	Effective date	Type	Version
Pain and Fever Relief - Pioneer Life Sciences, LLC	Pioneer Life Sciences, LLC	2021-05-18	HUMAN OTC DRUG LABEL	1