NDC 24208-299

Lotemax 5 mg per 1 mL suspension/ drops

On the label: Bausch & Lomb Incorporated.

United States: 1

Where it's made

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

Product details

Generic drug
Loteprednol: every company that makes it
Form
suspension/ drops, ophthalmic
Strength
5 mg per 1 mL
Approval
NDA NDA020583
On the market since
Mar 9, 1998
Package NDCs
24208-299-01 24208-299-05 24208-299-10 24208-299-15
Official label
DailyMed (National Library of Medicine), updated Apr 17, 2023

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