NDC 33261-019-10 - CELEBREX

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: 33261-019
Requested NDC: 33261-019-10
Package NDCs from labels: 33261-019-10, 33261-019-34, 33261-019-30, 33261-019-60
Manufacturer: Aidarex Pharmaceuticals LLC
Effective date: 2012-09-12
Current FDA listing: Not matched in FDA.report NDC product tables

DailyMed Labels#

Label, Manufacturer, Effective date table
Label	Manufacturer	Effective date	Type
CELEBREX - Aidarex Pharmaceuticals LLC	Aidarex Pharmaceuticals LLC	2012-09-12	HUMAN PRESCRIPTION DRUG LABEL

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
33261-019-30	2020-01-31	C162847	48780-1	9d75b9cf-d805-f424-e053-dadaa90a57ce	These highlights do not include all the information needed to use CELEBREX safely and effectively. See full prescribing information for CELEBREX. CELEBREX ® (celecoxib) capsules Initial U.S. Approval: 1998
33261-019-34	2020-01-31	C162847	48780-1	9d75b9cf-d805-f424-e053-dadaa90a57ce	These highlights do not include all the information needed to use CELEBREX safely and effectively. See full prescribing information for CELEBREX. CELEBREX ® (celecoxib) capsules Initial U.S. Approval: 1998
33261-019-60	2020-01-31	C162847	48780-1	9d75b9cf-d805-f424-e053-dadaa90a57ce	These highlights do not include all the information needed to use CELEBREX safely and effectively. See full prescribing information for CELEBREX. CELEBREX ® (celecoxib) capsules Initial U.S. Approval: 1998

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDC	Product	Description	Form	Quantity	SPL version
33261-019-10	CELEBREX	10 in 1 BOTTLE, PLASTIC	CAPSULE	10	1
33261-019-30	CELEBREX	30 in 1 BOTTLE, PLASTIC	CAPSULE	30	1
33261-019-34	CELEBREX	10 in 1 CARTON	CAPSULE	10	1
33261-019-60	CELEBREX	60 in 1 BOTTLE, PLASTIC	CAPSULE	60	1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
33261-019	CELEBREX (CELECOXIB) CAPSULE [AIDAREX PHARMACEUTICALS LLC]	1	Legacy NDC, 4 package rows	20120913_814511c9-89ef-42d7-912e-c00147833b7e.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDC	Billing unit	Product NDC	DailyMed indexing SPL	SPL version	Effective
33261-019-10	EA - Each	33261-019	2d59dde0-26e3-486c-a6e0-14d42fb4bc5b	1	2015-10-02
33261-019-30	EA - Each	33261-019	37d175b5-dd8d-4196-95f9-512e3419bf00	1	2015-10-02
33261-019-60	EA - Each	33261-019	8e8ccf32-0c3c-45df-b10f-4f9ef51c35ab	1	2015-10-02

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version
CELECOXIB	ACTIVE INGREDIENT	JCX84Q7J1L	CELEBREX (CELECOXIB) CAPSULE [AIDAREX PHARMACEUTICALS LLC]	1
CELECOXIB	ACTIVE MOIETY	JCX84Q7J1L	CELEBREX (CELECOXIB) CAPSULE [AIDAREX PHARMACEUTICALS LLC]	1
CROSCARMELLOSE SODIUM	INACTIVE INGREDIENT	M28OL1HH48	CELEBREX (CELECOXIB) CAPSULE [AIDAREX PHARMACEUTICALS LLC]	1
GELATIN	INACTIVE INGREDIENT	2G86QN327L	CELEBREX (CELECOXIB) CAPSULE [AIDAREX PHARMACEUTICALS LLC]	1
LACTOSE MONOHYDRATE	INACTIVE INGREDIENT	EWQ57Q8I5X	CELEBREX (CELECOXIB) CAPSULE [AIDAREX PHARMACEUTICALS LLC]	1
MAGNESIUM STEARATE	INACTIVE INGREDIENT	70097M6I30	CELEBREX (CELECOXIB) CAPSULE [AIDAREX PHARMACEUTICALS LLC]	1
POVIDONES	INACTIVE INGREDIENT	FZ989GH94E	CELEBREX (CELECOXIB) CAPSULE [AIDAREX PHARMACEUTICALS LLC]	1
SODIUM LAURYL SULFATE	INACTIVE INGREDIENT	368GB5141J	CELEBREX (CELECOXIB) CAPSULE [AIDAREX PHARMACEUTICALS LLC]	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 1 of 10 · 200 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Leader Artificial Tears 15 mL	POLYVINYL ALCOHOL, POVIDONE	Cardinal Health	8cccc589-3a8e-baad-e053-2a95a90ab8c7	2026-09-09	Warnings	Exact identifier unii: FZ989GH94E
FRESHKOTE PRESERVATIVE FREE LUBRICANT EYE DROPS	POVIDONE, POLYVINYL ALCOHOL SOLUTION	Harrow Eye, LLC	049e9cc9-0663-53bc-e063-6294a90a2c4f	2026-09-04	Warnings	Exact identifier unii: FZ989GH94E
Celecoxib	CELECOXIB	Major Pharmaceuticals	3a1eadd5-c0a7-473e-bde0-6b9450d11c95	2026-09-02	Boxed warning, Warnings, Adverse reactions	Exact identifier rxcui: 205323 unii: JCX84Q7J1L
Celecoxib	CELECOXIB	REMEDYREPACK INC.	c96509cc-47f4-44f8-9f7e-4e49cc3d5348	2026-08-28	Boxed warning, Warnings, Adverse reactions	Exact identifier rxcui: 205323 unii: JCX84Q7J1L
Celecoxib	CELECOXIB	DirectRx	e0f3aacf-df5d-dad7-e053-2995a90ac5eb	2026-08-27	Warnings, Adverse reactions	Exact identifier rxcui: 205323 unii: JCX84Q7J1L
Celecoxib	CELECOXIB	A-S Medication Solutions	e84d67c8-010d-495c-8691-ae16d0698f8d	2026-08-25	Boxed warning, Warnings, Adverse reactions	Exact identifier unii: JCX84Q7J1L
Celecoxib	CELECOXIB	St. Mary's Medical Park Pharmacy	59f495e8-3cea-9d98-e063-6394a90a89d4	2026-08-25	Boxed warning, Warnings, Adverse reactions	Exact identifier unii: JCX84Q7J1L
Rohto Optic Glow	NAPHAZOLINE HYDROCHLORIDE, POVIDONE, PROPYLENE GLYCOL	The Mentholatum Company	df9c5f7c-96e6-4b2b-b8cb-21a6a3342dff	2026-08-20	Warnings	Exact identifier unii: FZ989GH94E
Celecoxib	CELECOXIB	Mullan Pharmaceutical Inc.	643e177f-216d-4dfa-824a-7516a488304e	2026-08-19	Boxed warning, Warnings, Adverse reactions	Exact identifier rxcui: 205323 unii: JCX84Q7J1L
Rohto Preservative Free Dry Aid	POVIDONE, PROPYLENE GLYCOL	The Mentholatum Company	f4b1974c-2412-45f6-b79d-88b8a0bcb608	2026-08-18	Warnings	Exact identifier unii: FZ989GH94E
Rohto Dry-Aid	POVIDONE, PROPYLENE GLYCOL	The Mentholatum Company	8ea5c6c9-48f4-406a-a2cb-9280c546d87d	2026-08-18	Warnings	Exact identifier unii: FZ989GH94E
Celecoxib	CELECOXIB	REMEDYREPACK INC.	b3acbfd9-a1c2-4aa6-b5f0-013cfad6cca8	2026-08-17	Boxed warning, Warnings, Adverse reactions	Exact identifier rxcui: 205323 unii: JCX84Q7J1L
Celecoxib	CELECOXIB	REMEDYREPACK INC.	e18d2fa4-4982-4e2a-af55-4319d6416efb	2026-08-14	Boxed warning, Warnings, Adverse reactions	Exact identifier rxcui: 205323 unii: JCX84Q7J1L
Celecoxib	CELECOXIB	A-S Medication Solutions	d799328f-9ea0-4b64-9667-8feaa97f150c	2026-08-07	Boxed warning, Warnings, Adverse reactions	Exact identifier unii: JCX84Q7J1L
Celecoxib	CELECOXIB	PD-Rx Pharmaceuticals, Inc.	b06ced10-81c6-4f48-a205-1e0db228cb8b	2026-08-03	Boxed warning, Warnings, Adverse reactions	Exact identifier rxcui: 205323 unii: JCX84Q7J1L
Celecoxib	CELECOXIB	Alembic Pharmaceuticals Inc.	806e5f8a-f986-4f88-ba3e-8265f86afa48	2026-07-31	Boxed warning, Warnings, Adverse reactions	Exact identifier rxcui: 205323 unii: JCX84Q7J1L
GOOD NEIGHBOR PHARMACY ARTIFICAL TEARS LUBRICANT EYE DROPS	POLYVINYL ALCOHOL, POVIDONE	AmerisourceBergen	ce6852a8-c5e6-403d-a7b4-a2e85d1ebb1f	2026-07-22	Warnings	Exact identifier unii: FZ989GH94E
CELECOXIB	CELECOXIB	REMEDYREPACK INC.	27f17ae7-939b-402e-9498-3b6611104089	2026-07-21	Boxed warning, Warnings, Adverse reactions	Exact identifier rxcui: 205323 unii: JCX84Q7J1L
Celecoxib	CELECOXIB	PD-Rx Pharmaceuticals, Inc.	06076494-62ad-4f58-b8bb-7038fcfe3b12	2026-07-17	Boxed warning, Warnings, Adverse reactions	Exact identifier rxcui: 205323 unii: JCX84Q7J1L
Celecoxib	CELECOXIB	St. Mary's Medical Park Pharmacy	3bc74e76-0517-69c6-e063-6394a90abe75	2026-07-17	Boxed warning, Warnings, Adverse reactions	Exact identifier unii: JCX84Q7J1L

Reported adverse events (FAERS/openFDA)#

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