NDC 24208-507

Lotemax SM 3.8 mg per 1 g gel

On the label: Bausch & Lomb Incorporated.

United States: 1

Where it's made

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

Product details

Generic drug
Loteprednol: every company that makes it
Form
gel, ophthalmic
Strength
3.8 mg per 1 g
Approval
NDA NDA208219
On the market since
Feb 25, 2019
Package NDCs
24208-507-01 24208-507-02 24208-507-07
Official label
DailyMed (National Library of Medicine), updated Mar 31, 2026

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