CELECOXIB
Generic: CELECOXIB
Westminster PharmaceuticalsManufacturer
ORALRoute
CELECOXIBActive Substance
2018-01-23Original Approval
CELECOXIB is FDA application ANDA210071, sponsored by CSPC OUYI. Any recalls listed below come from FDA drug enforcement reports, and reaction counts are the number of FAERS adverse event reports that mention the drug and that reaction; a report does not prove the drug caused it.
Recalls
Class II2025-05-09
Celecoxib Capsules, 200 mg, 500-count bottle, Rx only, Manufactured by: Alembic Pharmaceuticals Limited (Formulation DivPresence of Foreign Tablets/Capsules; customer complaint found one Tadalafil 5mg tablet inside a sea
Class II2025-05-13
Celecoxib Capsules, 200 mg, 50 Capsules (5x10) Unit Dose per carton, Rx Only, Manufactured for: AvKARE, Pulaski, TN 3847Presence of Foreign Tablets/Capsules: manufacturer recalled because one tadalafil 5mg tablet was fou
Top Reported Reactions
1
DRUG INEFFECTIVE
5,326 reports
2
OFF LABEL USE
3,336 reports
3
FATIGUE
3,270 reports
4
ARTHRALGIA
3,227 reports
5
PAIN
3,207 reports
6
NAUSEA
3,158 reports
7
DIARRHOEA
2,847 reports
8
VOMITING
2,577 reports
9
RHEUMATOID ARTHRITIS
2,492 reports
10
RASH
2,466 reports