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Two medicines, side by side

Celecoxib vs etodolac

Celecoxib and etodolac are both labeled for pain, osteoarthritis and rheumatoid arthritis. Drugs@FDA records approvals of celecoxib since 1998 and of etodolac since 1991. Pharmacies paid $0.0762 per celecoxib 200 mg capsule and $0.262 per etodolac 400 mg tablet (NADAC, October 7, 2026); the strengths differ, so the two prices are not like for like. How each works, in its label's words: Celecoxib, “The mechanism of action of CELEBREX is believed to be due to inhibition of prostaglandin synthesis, primarily via inhibition of COX-2.”; Etodolac, “of etodolac, like that of other NSAIDs, is not completely understood, but may be related to prostaglandin synthetase inhibition.”

Check it at the source: the celecoxib FDA label on DailyMed (effective November 22, 2024); the etodolac FDA label on DailyMed (effective July 16, 2026).

Highlights of the celecoxib record

Celecoxib (Celebrex) · label of November 22, 2024

Boxed warning

RISK OF SERIOUS CARDIOVASCULAR AND GASTROINTESTINAL EVENTS Cardiovascular Thrombotic Events

Nonsteroidal anti-inflammatory drugs (NSAIDs) cause an increased risk of serious cardiovascular thrombotic events, including myocardial infarction, and stroke, which can be fatal. This risk may occur early in the treatment and may increase with duration of use [see Warnings and Precautions (5.1) ].

Used for

From the label: indications

CELEBREX is a nonsteroidal anti-inflammatory drug indicated for: • Osteoarthritis (OA) ( 1.1 ) • Rheumatoid Arthritis (RA) ( 1.2 ) • Juvenile Rheumatoid Arthritis (JRA) in patients 2 years and older ( 1.3 ) • Ankylosing Spondylitis (AS) ( 1.4 ) • Acute Pain (AP) ( 1.5 ) • Primary Dysmenorrhea (PD) ( 1.6 ) 1.1 Osteoarthritis (OA) For the management of the signs and symptoms of OA [see Clinical Studies (14.1) ]. 1.2 […]

On the market

Earliest approval on file
December 31, 1998
Generic labelers
63 labelers
Pharmacy cost
$0.0762 per capsule

Supply and safety

Shortage
No current entry
Recalls
2

Highlights of the etodolac record

Etodolac (Lodine) · label of July 16, 2026

Boxed warning

Cardiovascular Thrombotic Events Nonsteroidal anti-inflammatory drugs (NSAIDs) cause an increased risk of serious cardiovascular thrombotic events, including myocardial infarction and stroke, which can be fatal. This risk may occur early in treatment and may increase with duration of use [see Warnings and Precautions ]. Etodolac tablets, 400 mg and 500 mg are contraindicated in the setting of coronary artery bypass graft (CABG) surgery [see Contraindications and Warnings ].

Used for

From the label: indications

Carefully consider the potential benefits and risks of etodolac tablets and other treatment options before deciding to use etodolac tablets. Use the lowest effective dose for the shortest duration consistent with individual patient treatment goals (see WARNINGS ). […]

On the market

Earliest approval on file
January 31, 1991
Generic labelers
30 labelers
Pharmacy cost
$0.262 per tablet

Supply and safety

Shortage
No current entry
Recalls
0

Source: FDA drug labels via openFDA (Celecoxib label of November 22, 2024, Etodolac label of July 16, 2026); NDC Directory, Drugs@FDA, NADAC, FDA shortages and recalls (October 8, 2026)

How do celecoxib and etodolac differ on the record?

How each works, in its label's words: Celecoxib, “The mechanism of action of CELEBREX is believed to be due to inhibition of prostaglandin synthesis, primarily via inhibition of COX-2.”; Etodolac, “of etodolac, like that of other NSAIDs, is not completely understood, but may be related to prostaglandin synthetase inhibition.”

Both are in FDA's class nonsteroidal anti-inflammatory drugs.

Half-life, in each label's words: Celecoxib, “It is primarily metabolized by CYP2C9 with a half-life of approximately 11 hours.”; Etodolac, “The terminal half-life (t 1/2 ) of etodolac is 6.4 hours (22% CV).”

Both labels carry a boxed warning; the records quote them.

Generics: celecoxib since 2014; etodolac since 1997 (Drugs@FDA).

CelecoxibEtodolac
Labeled forOsteoarthritis, Rheumatoid arthritis, Pain, MigrainePain, Osteoarthritis, Rheumatoid arthritis
Pharmacologic classNonsteroidal Anti-inflammatory DrugNonsteroidal Anti-inflammatory Drug
How it works (label)Celecoxib has analgesic, anti-inflammatory, and antipyretic properties. The mechanism of action of CELEBREX is believed to be due to inhibition of prostaglandin synthesis, primarily via inhibition of COX-2.of etodolac, like that of other NSAIDs, is not completely understood, but may be related to prostaglandin synthetase inhibition. Etodolac is a racemic mixture of [-]R- and [+]S-etodolac.
Half-life (label)It is primarily metabolized by CYP2C9 with a half-life of approximately 11 hours.The terminal half-life (t 1/2 ) of etodolac is 6.4 hours (22% CV).
Earliest approval on file (Drugs@FDA)December 31, 1998January 31, 1991
First generic approvedMay 30, 2014February 28, 1997
Generic labelers (NDC)63 labelers30 labelers
Pharmacy cost (NADAC, each one's most listed form; strengths differ)$0.0762 per capsule (Celecoxib 200 mg capsule)$0.262 per tablet (Etodolac 400 mg tablet)
12-month price change-13%+0.9%
Boxed warningYesYes
Shortage nowNo current entryNo current entry
Recalls recorded20
FAERS reports (a report is not proof of cause; counts follow how widely a medicine is used)130,8825,958
DEA schedulenonenone

Source: Drugs@FDA, FDA NDC Directory, CMS NADAC of October 7, 2026, FDA shortages and recalls, FAERS via openFDA (FDA files October 8, 2026)

What do the labels say about using others of their kind?

Celecoxib label, drug interactions

Concomitant use of Celecoxib with other NSAIDs or salicylates (e.g., diflunisal, salsalate) increases the risk of GI toxicity, with little or no increase in efficacy [see Warnings and Precautions (5.2) ].

Etodolac label, drug interactions

The clinical significance of this interaction is not known; however, as with other NSAIDs, concomitant administration of etodolac and aspirin is not generally recommended because of the potential of increased adverse effects.

Source: FDA drug labels via openFDA

What next?

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