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 10 of 10 · 199 matching rows.

Brand, Generic, Manufacturer table
Brand	Generic	Manufacturer	SPL set ID	Effective date	Available safety fields	Join
Celecoxib	CELECOXIB	Proficient Rx LP	c529b321-38ed-434f-b76e-06902cdd40dc	2023-12-01	Boxed warning, Warnings, Adverse reactions	Exact identifier unii: JCX84Q7J1L
celecoxib	CELECOXIB	Asclemed USA, Inc.	2a926010-08e1-44dd-bc6d-ed15374bd0d3	2023-09-02	Boxed warning, Warnings, Adverse reactions	Exact identifier rxcui: 205323 unii: JCX84Q7J1L
CELECOXIB	CELECOXIB	A-S Medication Solutions	00e67d5e-df6f-4dfd-8c2d-a001c8a99af0	2023-08-24	Boxed warning, Warnings, Adverse reactions	Exact identifier rxcui: 205323 unii: JCX84Q7J1L
Household Antigens	ACETONE, SODIUM TRIPOLYPHOSPHATE, PROPYLENE GLYCOL, BENZINUM, AMMONIUM MURIATICUM, SODIUM LAURYL SULFATE, TEREBINTHINA, ANACARDIUM ORIENTALE, GRAPHITES, NITRICUM ACIDUM, PULSATILLA (PRATENSIS), SULPHUR	BioActive Nutritional	3382df85-3ec5-4371-830e-4ed345b8f51b	2023-07-14	Warnings	Exact identifier unii: 368GB5141J
Pneumotox	TRITICUM AESTIVUM, ALFALFA, ARNICA MONTANA, ASCLEPIAS TUBEROSA, CHAMOMILLA, ECHINACEA (ANGUSTIFOLIA), EUCALYPTUS GLOBULUS, FUCUS VESICULOSUS, HORDEUM VULGARE, IODIUM, NASTURTIUM AQUATICUM, PLANTAGO MAJOR, RAPHANUS SATIVUS, TRIFOLIUM PRATENSE, TRIGONELLA FOENUM-GRAECUM, SYMPHYTUM OFFICINALE, LUNG (SUIS), ORYZA SATIVA, SILICEA, ACETONE, SODIUM TRIPOLYPHOSPHATE, PROPYLENE GLYCOL, BENZINUM, AMMONIUM MURIATICUM, SODIUM LAURYL SULFATE, TEREBINTHINA, ARSENICUM ALBUM, NATRUM MURIATICUM, NITRICUM ACIDUM,	BioActive Nutritional, Inc.	f8846fb1-92e5-4f8e-b3b3-bc620df90a62	2023-07-12	Warnings	Exact identifier unii: 368GB5141J
Celecoxib	CELECOXIB	Proficient Rx LP	b9a7f32c-8136-4f29-be6b-4d5e904ca0f1	2023-05-01	Boxed warning, Warnings, Adverse reactions	Exact identifier rxcui: 205323 unii: JCX84Q7J1L
CELECOXIB	CELECOXIB	A-S Medication Solutions	c7a183dc-f4d5-483f-964c-f2745a3640ad	2023-02-28	Boxed warning, Warnings, Adverse reactions	Exact identifier unii: JCX84Q7J1L
celecoxib	CELECOXIB	A-S Medication Solutions	85bfe02b-bfcb-44ee-81a0-11765c3054a9	2023-02-06	Boxed warning, Warnings, Adverse reactions	Exact identifier rxcui: 205323 unii: JCX84Q7J1L
Petrochemical Detox	CHELIDONIUM MAJUS, TARAXACUM OFFICINALE, TRIFOLIUM PRATENSE, SYMPHYTUM OFFICINALE, ACETONE, SODIUM TRIPOLYPHOSPHATE, PROPYLENE GLYCOL, BENZINUM, AMMONIUM MURIATICUM, SODIUM LAURYL SULFATE, TEREBINTHINA, ARSENICUM ALBUM, CADMIUM SULPHURATUM, GELSEMIUM SEMPERVIRENS, IRIDIUM METALLICUM, LYCOPODIUM CLAVATUM, MERCURIUS SOLUBILIS, NITRICUM ACIDUM, NUX VOMICA, PETROLEUM, PHOSPHORICUM ACIDUM, PLATINUM METALLICUM, LATRODECTUS MACTANS	Deseret Biologicals, Inc.	b38b492a-cf45-4aa2-ba7e-4573d2c4ebe5	2023-01-12	Warnings	Exact identifier unii: 368GB5141J
celecoxib	CELECOXIB	Proficient Rx LP	0ad14a4e-2f05-4ce7-93d1-1cb7e4d8f7d0	2022-08-01	Boxed warning, Warnings, Adverse reactions	Exact identifier unii: JCX84Q7J1L
celecoxib	CELECOXIB	Proficient Rx LP	cbd2d6de-6f0d-4b69-8e27-a1fe08830ba5	2022-04-01	Boxed warning, Warnings, Adverse reactions	Exact identifier rxcui: 205323 unii: JCX84Q7J1L
Celecoxib	CELECOXIB	Tianjin Tianyao Pharmaceuticals Co., Ltd.	76f9bcb7-0e94-485f-816d-61d4e1ed24e0	2022-02-28	Boxed warning, Warnings, Adverse reactions	Exact identifier rxcui: 205323 unii: JCX84Q7J1L
Celecoxib	CELECOXIB	Aphena Pharma Solutions - Tennessee, LLC	d258e065-e9a6-44e2-89c9-6892d771d9d3	2021-08-09	Boxed warning, Warnings, Adverse reactions	Exact identifier rxcui: 205323 unii: JCX84Q7J1L
CELECOXIB	CELECOXIB	Proficient Rx LP	c91e5933-1798-4096-9f08-fb1200e154e1	2021-01-01	Boxed warning, Warnings, Adverse reactions	Exact identifier unii: JCX84Q7J1L
Celecoxib	CELECOXIB	Proficient Rx LP	6dd743d3-4821-4919-90eb-6d306ca7999f	2021-01-01	Boxed warning, Warnings, Adverse reactions	Exact identifier rxcui: 205323 unii: JCX84Q7J1L
Celecoxib 200 mg	CELECOXIB	Proficient Rx LP	feee6a01-63f9-42c3-8bd8-ca713a08b36d	2019-11-01	Boxed warning, Warnings, Adverse reactions	Exact identifier rxcui: 205323 unii: JCX84Q7J1L
Celecoxib	CELECOXIB	Proficient Rx LP	7a234c0c-30a7-49f5-92a1-a1fc836ff9ae	2019-10-01	Boxed warning, Warnings, Adverse reactions	Exact identifier unii: JCX84Q7J1L
Celecoxib	CELECOXIB	Proficient Rx LP	c787b0ab-77ab-4f7e-9fea-be2a0085020a	2019-10-01	Boxed warning, Warnings, Adverse reactions	Exact identifier rxcui: 205323 unii: JCX84Q7J1L
bcb89362-3e1a-41ed-ba17-d740662897e0			814511c9-89ef-42d7-912e-c00147833b7e	2012-09-12	Boxed warning, Warnings, Adverse reactions	Exact identifier spl id: bcb89362-3e1a-41ed-ba17-d740662897e0 spl set id: 814511c9-89ef-42d7-912e-c00147833b7e

Reported adverse events (FAERS/openFDA)#

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