NDC 31722-342-01 - Naproxen

This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.

Product NDC: 31722-342
Requested NDC: 31722-342-01
Package NDCs from labels: 31722-342-10, 31722-342-50, 31722-342-01, 31722-342-05
Manufacturer: Camber Pharmaceuticals | Invagen Pharmaceuticals
Effective date: 2025-09-03
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
Naproxen - Camber Pharmaceuticals \| Invagen Pharmaceuticals	Camber Pharmaceuticals \| Invagen Pharmaceuticals	2025-09-03	HUMAN PRESCRIPTION DRUG LABEL
NAPROXEN - DirectRX	DirectRX	2020-01-21	HUMAN PRESCRIPTION DRUG LABEL
Naproxen - St. Mary's Medical Park Pharmacy \| Invagen Pharmaceuticals	St. Mary's Medical Park Pharmacy \| Invagen Pharmaceuticals	2018-11-15	HUMAN PRESCRIPTION DRUG LABEL
Naproxen Tablets, USP	Blenheim Pharmacal, Inc.	2015-12-11	HUMAN PRESCRIPTION DRUG LABEL
Naproxen - State of Florida DOH Central Pharmacy	State of Florida DOH Central Pharmacy	2014-10-21	HUMAN PRESCRIPTION DRUG LABEL
National Council for Prescription Drug Programs indexing - billing unit	National Council for Prescription Drug Programs	2012-07-24	Indexing - Billing Unit

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Related label table
NDC	Effective	Related label
31722-342-05	2025-09-05	Naproxen Tablets, USP
31722-342-50	2025-09-05	Naproxen Tablets, USP
31722-342-05	2019-11-13	Naproxen Tablets, USP
31722-342-50	2019-11-13	Naproxen Tablets, USP

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
31722-342	NAPROXEN TABLET [CAMBER PHARMACEUTICALS]	1	Legacy NDC	20120201_8dd7fade-d750-49ce-b798-a1d3615e57b7.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
31722-342-01	EA - Each	31722-342	985e3d05-aaab-4fb1-a08e-08608cdd8ce5	1	2012-07-24
31722-342-05	EA - Each	31722-342	bff54d3a-d4b3-408a-ad96-f3763180cf67	1	2012-07-24

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
NAPROXEN	ACTIVE INGREDIENT	57Y76R9ATQ	NAPROXEN TABLET [BLENHEIM PHARMACAL, INC.]	2
NAPROXEN	ACTIVE INGREDIENT	57Y76R9ATQ	NAPROXEN TABLET [DIRECTRX]	2
NAPROXEN	ACTIVE INGREDIENT	57Y76R9ATQ	NAPROXEN TABLET [STATE OF FLORIDA DOH CENTRAL PHARMACY]	2
NAPROXEN	ACTIVE MOIETY	57Y76R9ATQ	NAPROXEN TABLET [BLENHEIM PHARMACAL, INC.]	2
NAPROXEN	ACTIVE MOIETY	57Y76R9ATQ	NAPROXEN TABLET [STATE OF FLORIDA DOH CENTRAL PHARMACY]	2
NAPROXEN	ACTIVE MOIETY	57Y76R9ATQ	NAPROXEN TABLET [DIRECTRX]	2
COLLOIDAL SILICON DIOXIDE	INACTIVE INGREDIENT	ETJ7Z6XBU4	NAPROXEN TABLET [STATE OF FLORIDA DOH CENTRAL PHARMACY]	2
CROSCARMELLOSE SODIUM	INACTIVE INGREDIENT	M28OL1HH48	NAPROXEN TABLET [BLENHEIM PHARMACAL, INC.]	2
CROSCARMELLOSE SODIUM	INACTIVE INGREDIENT	M28OL1HH48	NAPROXEN TABLET [DIRECTRX]	2
CROSCARMELLOSE SODIUM	INACTIVE INGREDIENT	M28OL1HH48	NAPROXEN TABLET [STATE OF FLORIDA DOH CENTRAL PHARMACY]	2
FERRIC OXIDE YELLOW	INACTIVE INGREDIENT	EX438O2MRT	NAPROXEN TABLET [BLENHEIM PHARMACAL, INC.]	2
FERRIC OXIDE YELLOW	INACTIVE INGREDIENT	EX438O2MRT	NAPROXEN TABLET [STATE OF FLORIDA DOH CENTRAL PHARMACY]	2
FERRIC OXIDE YELLOW	INACTIVE INGREDIENT	EX438O2MRT	NAPROXEN TABLET [DIRECTRX]	2
MAGNESIUM STEARATE	INACTIVE INGREDIENT	70097M6I30	NAPROXEN TABLET [BLENHEIM PHARMACAL, INC.]	2
MAGNESIUM STEARATE	INACTIVE INGREDIENT	70097M6I30	NAPROXEN TABLET [STATE OF FLORIDA DOH CENTRAL PHARMACY]	2
MAGNESIUM STEARATE	INACTIVE INGREDIENT	70097M6I30	NAPROXEN TABLET [DIRECTRX]	2
POVIDONE	INACTIVE INGREDIENT	FZ989GH94E	NAPROXEN TABLET [BLENHEIM PHARMACAL, INC.]	2
POVIDONE	INACTIVE INGREDIENT	FZ989GH94E	NAPROXEN TABLET [DIRECTRX]	2
POVIDONES	INACTIVE INGREDIENT	FZ989GH94E	NAPROXEN TABLET [STATE OF FLORIDA DOH CENTRAL PHARMACY]	2
SILICON DIOXIDE	INACTIVE INGREDIENT	ETJ7Z6XBU4	NAPROXEN TABLET [BLENHEIM PHARMACAL, INC.]	2
SILICON DIOXIDE	INACTIVE INGREDIENT	ETJ7Z6XBU4	NAPROXEN TABLET [DIRECTRX]	2
NAPROXEN	ACTIVE INGREDIENT	57Y76R9ATQ	NAPROXEN TABLET [ST. MARY'S MEDICAL PARK PHARMACY]	1
NAPROXEN	ACTIVE INGREDIENT	57Y76R9ATQ	NAPROXEN TABLET [CAMBER PHARMACEUTICALS]	1
NAPROXEN	ACTIVE MOIETY	57Y76R9ATQ	NAPROXEN TABLET [ST. MARY'S MEDICAL PARK PHARMACY]	1
NAPROXEN	ACTIVE MOIETY	57Y76R9ATQ	NAPROXEN TABLET [CAMBER PHARMACEUTICALS]	1
CROSCARMELLOSE SODIUM	INACTIVE INGREDIENT	M28OL1HH48	NAPROXEN TABLET [ST. MARY'S MEDICAL PARK PHARMACY]	1
CROSCARMELLOSE SODIUM	INACTIVE INGREDIENT	M28OL1HH48	NAPROXEN TABLET [CAMBER PHARMACEUTICALS]	1
FERRIC OXIDE RED	INACTIVE INGREDIENT	1K09F3G675	NAPROXEN TABLET [CAMBER PHARMACEUTICALS]	1
FERRIC OXIDE YELLOW	INACTIVE INGREDIENT	EX438O2MRT	NAPROXEN TABLET [CAMBER PHARMACEUTICALS]	1
FERRIC OXIDE YELLOW	INACTIVE INGREDIENT	EX438O2MRT	NAPROXEN TABLET [ST. MARY'S MEDICAL PARK PHARMACY]	1
MAGNESIUM STEARATE	INACTIVE INGREDIENT	70097M6I30	NAPROXEN TABLET [ST. MARY'S MEDICAL PARK PHARMACY]	1
MAGNESIUM STEARATE	INACTIVE INGREDIENT	70097M6I30	NAPROXEN TABLET [CAMBER PHARMACEUTICALS]	1
POVIDONE	INACTIVE INGREDIENT	FZ989GH94E	NAPROXEN TABLET [ST. MARY'S MEDICAL PARK PHARMACY]	1
POVIDONE	INACTIVE INGREDIENT	FZ989GH94E	NAPROXEN TABLET [CAMBER PHARMACEUTICALS]	1
SILICON DIOXIDE	INACTIVE INGREDIENT	ETJ7Z6XBU4	NAPROXEN TABLET [ST. MARY'S MEDICAL PARK PHARMACY]	1
SILICON DIOXIDE	INACTIVE INGREDIENT	ETJ7Z6XBU4	NAPROXEN TABLET [CAMBER PHARMACEUTICALS]	1

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 20 of 44 · 863 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
NAPROXEN	NAPROXEN	PD-Rx Pharmaceuticals, Inc.	a9f9ce81-9d51-4167-9581-974866a8fe31	2025-10-17	Warnings	Exact identifier rxcui: 198014 unii: 57Y76R9ATQ
Naproxen and esomeprazole magnesium	NAPROXEN AND ESOMEPRAZOLE MAGNESIUM	Preferred Pharmaceuticals Inc.	6368a3be-4b79-466b-8ec4-11fc3ac623cc	2025-10-17	Boxed warning, Warnings, Adverse reactions	Exact identifier unii: 57Y76R9ATQ
DENTI BUONGIORNO PEACH MINT WHITENING TOOTH	HYDROGEN PEROXIDE, SILICA	ATOSAFE CO., Ltd	41196c2f-8e2e-a54d-e063-6294a90ad8a7	2025-10-14	Warnings	Exact identifier unii: ETJ7Z6XBU4
DENTI BUONGIORNO PEACH MINT WHITENING TOOTH	HYDROGEN PEROXIDE, SILICA	DONG IL PHARMS CO.,LTD	41198822-7c8f-ceb2-e063-6394a90a4373	2025-10-14	Warnings	Exact identifier unii: ETJ7Z6XBU4
DENTI BUONGIORNO ORIGINAL TOOTH	SILICA, SODIUM MONOFLUOROPHOSPHATE	DONG IL PHARMS CO.,LTD	41197bb6-f6f4-c86d-e063-6294a90ad476	2025-10-14	Warnings	Exact identifier unii: ETJ7Z6XBU4
DENTI BUONGIORNO ORIGINAL TOOTH	SILICA, SODIUM MONOFLUOROPHOSPHATE	ATOSAFE CO., Ltd	4114ab09-1115-6b0b-e063-6394a90ab442	2025-10-13	Warnings	Exact identifier unii: ETJ7Z6XBU4
DENTI BUONGIORNO PLAQUE CARE TOOTH	SILICA, SODIUM FLUORIDE, TOCOPHERYL ACETATE, TETRASODIUM PYROPHOSPHATE	ATOSAFE CO., Ltd	41155922-d7ac-0a7a-e063-6294a90afe48	2025-10-13	Warnings	Exact identifier unii: ETJ7Z6XBU4
DENTI BUONGIORNO PLAQUE CARE TOOTH	SILICA, SODIUM FLUORIDE, TOCOPHERYL ACETATE, TETRASODIUM PYROPHOSPHATE	DONG IL PHARMS CO.,LTD	41157552-2473-176b-e063-6294a90a9ad0	2025-10-13	Warnings	Exact identifier unii: ETJ7Z6XBU4
DENTI BUONGIORNO GUM CARE TOOTH	SILICA, SODIUM FLUORIDE, TOCOPHERYL ACETATE	ATOSAFE CO., Ltd	4115d122-3090-d3e5-e063-6294a90aafb6	2025-10-13	Warnings	Exact identifier unii: ETJ7Z6XBU4
DENTI BUONGIORNO GUM CARE TOOTH	SILICA, SODIUM FLUORIDE, TOCOPHERYL ACETATE	DONG IL PHARMS CO.,LTD	4115b653-63ff-703f-e063-6294a90a652a	2025-10-13	Warnings	Exact identifier unii: ETJ7Z6XBU4
Naproxen	NAPROXEN	Bryant Ranch Prepack	e0f430fd-4511-41c8-b5e9-894abe4f3c37	2025-10-13	Boxed warning, Warnings, Adverse reactions	Exact identifier rxcui: 198014 unii: 57Y76R9ATQ
Silicea Belladonna	SILICEA BELLADONNA	Uriel Pharmacy Inc.	a142eb87-c5fb-4138-bc98-e7f1391fe221	2025-10-10	Warnings	Exact identifier unii: ETJ7Z6XBU4
Naproxen	NAPROXEN	A-S Medication Solutions	cfa88511-40bb-4658-b606-44c68d0746b7	2025-10-08	Boxed warning, Warnings, Adverse reactions	Exact identifier rxcui: 198014 unii: 57Y76R9ATQ
Naproxen	NAPROXEN	A-S Medication Solutions	b500bdba-946a-41ff-855c-1f2937547d01	2025-10-08	Boxed warning, Warnings, Adverse reactions	Exact identifier rxcui: 198014 unii: 57Y76R9ATQ
Naproxen	NAPROXEN	Aurobindo Pharma Limited	570974d4-0d5b-4df2-b307-37380511835d	2025-10-07	Boxed warning, Warnings, Adverse reactions	Exact identifier unii: 57Y76R9ATQ
Parathyropar	SYMPHYTUM OFFICINALE, BARYTA CARBONICA, CALCAREA CARBONICA, CALCAREA PHOSPHORICA, HEKLA LAVA, MANGANUM METALLICUM, RHUS TOX, SILICEA, PARATHORMONUM	Energique, Inc.	bd13617a-c470-4421-8f47-43a98036f40b	2025-10-06	Warnings	Exact identifier unii: ETJ7Z6XBU4
Mitochondria PRO	ARALIA QUINQUEFOLIA, ARNICA MONTANA, ADENOSINUM TRIPHOSPHORICUM DINATRUM, ALPHA-KETOGLUTARICUM ACIDUM, ASCORBICUM ACIDUM, ALPHA-LIPOICUM ACIDUM, CALCAREA CARBONICA, CITRICUM ACIDUM, CUPRUM METALLICUM, CYSTEINUM, FERRUM METALLICUM, IODIUM, LEVOTHYROXINUM, MAGNESIUM GLUCONICUM DIHYDRICUM, MALICUM ACIDUM, MANGANUM ACETICUM, NADIDUM, NATRUM PYRUVICUM, NICOTINAMIDUM, PYRIDOXINUM HYDROCHLORICUM, RIBOFLAVINUM, SELENIUM METALLICUM, SULPHUR, THIAMINUM HYDROCHLORICUM, UBIDECARENONUM, ZINCUM METALLICUM,	Energique, Inc.	8c3e961d-bc33-40cd-a282-a4fe5aa3f0ad	2025-10-06	Warnings	Exact identifier unii: ETJ7Z6XBU4
Tri-Relief Antifungal	SODIUM CHLORIDE, SILICON DIOXIDE, AND THUJA OCCIDENTALIS LEAFY TWIG	Forces of Nature	6fe97b54-8aa3-4d86-9055-0629589a416b	2025-10-06	Warnings	Exact identifier unii: ETJ7Z6XBU4
Naproxen	NAPROXEN	PD-Rx Pharmaceuticals, Inc.	2d01e583-670a-46f4-b5f2-3fad46d0376f	2025-10-02	Boxed warning, Warnings, Adverse reactions	Exact identifier unii: 57Y76R9ATQ
Cloveden Vegan Whitening Tooth	SILICA, HYDROGEN PEROXIDE, TOCOPHERYL ACETATE	DONG IL PHARMS CO.,LTD	3fb16579-7cf1-873a-e063-6294a90a9ac1	2025-09-26	Warnings	Exact identifier unii: ETJ7Z6XBU4

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.