NAFTIFINE HYDROCHLORIDE
Generic: NAFTIFINE HYDROCHLORIDE
Sun Pharmaceutical IndustriesManufacturer
TOPICALRoute
NAFTIFINE HYDROCHLORIDEActive Substance
2016-01-06Original Approval
NAFTIFINE HYDROCHLORIDE is FDA application ANDA206901, sponsored by SUN PHARMA CANADA. 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.
Top Reported Reactions
1
PRURITUS
7 reports
2
ERYTHEMA
5 reports
3
SKIN EXFOLIATION
5 reports
4
BLISTER
4 reports
5
HAEMORRHAGE
4 reports
6
HYPERSENSITIVITY
4 reports
7
SKIN BURNING SENSATION
4 reports
8
SKIN DISCOLOURATION
4 reports
9
SKIN HYPERTROPHY
4 reports
10
SKIN WRINKLING
4 reports