NDC 24208-443

Lotemax 5 mg per 1 g ointment

On the label: Bausch & Lomb Incorporated.

United States: 1

Where it's made

FactoryWhereRoleLast FDA inspection
Bausch & Lomb IncorporatedTampa, FL, United StatesMakes it and packages it Serious problems, FDA actionMar 20, 2026 · 17 inspections, 3 with FDA action

Product details

Generic drug
Loteprednol: every company that makes it
Form
ointment, ophthalmic
Strength
5 mg per 1 g
Approval
NDA NDA200738
On the market since
Apr 15, 2011
Package NDCs
24208-443-01 24208-443-35
Official label
DailyMed (National Library of Medicine), updated Nov 30, 2022

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