NALTREXONE HYDROCHLORIDE
Generic: NALTREXONE HYDROCHLORIDE
Elite LaboratoriesManufacturer
ORALRoute
NALTREXONE HYDROCHLORIDEActive Substance
1999-05-26Original Approval
NALTREXONE HYDROCHLORIDE is FDA application ANDA075274, sponsored by ELITE LABS. 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
FATIGUE
172 reports
2
DRUG INEFFECTIVE
149 reports
3
INSOMNIA
116 reports
4
NAUSEA
107 reports
5
HEADACHE
100 reports
6
PAIN
83 reports
7
PRODUCT DOSE OMISSION ISSUE
82 reports
8
WEIGHT INCREASED
78 reports
9
MALAISE
71 reports
10
POOR QUALITY SLEEP
71 reports