OTC
Strength
.25 mg/mL
Manufacturer
Bausch & Lomb IncorporatedNDC
24208060110
Classification
Brand
Dosage Form
SOLUTION/ DROPS
Route
OPHTHALMIC
Last Updated
9/17/2025
Active Ingredients
KETOTIFEN FUMARATEApproval Type
New Drug (NDA)
FDA Application
NDA021996On Market Since
12/1/2006
Pharmacological Classes
Histamine H1 Receptor Antagonists
Histamine-1 Receptor Inhibitor
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