NDC 24208-377

Miebo 1 mg per 1 mg solution

On the label: Bausch & Lomb Incorporated.

United States: 1

Where it's made

FactoryWhereRoleLast FDA inspection
Alliance Medical Products, Inc. (dba Siegfried Irvine)Irvine, CA, United StatesMakes it Problems found, fixed voluntarilyNov 7, 2025 · 12 inspections
Bausch & Lomb IncorporatedTampa, FL, United StatesPackages it Serious problems, FDA actionMar 20, 2026 · 17 inspections, 3 with FDA action

Product details

Generic drug
Perfluorohexyloctane: every company that makes it
Form
solution, ophthalmic
Strength
1 mg per 1 mg
Approval
NDA NDA216675
On the market since
May 18, 2023
Package NDCs
24208-377-01 24208-377-05 24208-377-06
Official label
DailyMed (National Library of Medicine), updated Mar 10, 2026

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