SULINDAC
Generic: SULINDAC
PuraCap Laboratories LLC dba Blu PharmaceuticalsManufacturer
ORALRoute
SULINDACActive Substance
1991-03-25Original Approval
SULINDAC is FDA application ANDA072711, sponsored by EPIC PHARMA. 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
Top Reported Reactions
1
DRUG INEFFECTIVE
214 reports
2
PAIN
185 reports
3
FATIGUE
154 reports
4
ARTHRALGIA
140 reports
5
NAUSEA
128 reports
6
PAIN IN EXTREMITY
114 reports
7
ASTHENIA
107 reports
8
DIARRHOEA
106 reports
9
HEADACHE
103 reports
10
BACK PAIN
97 reports