NDC 24208-377 – Miebo

Perfluorohexyloctane 1 mg/mg · Solution · Ophthalmic

Human Prescription Drug

Product NDC24208-377

Product details

Brand name
Miebo
Generic name
Perfluorohexyloctane
Labeler
Bausch & Lomb Incorporated
Dosage form
Solution
Route
Ophthalmic
Marketing category
NDA · NDA216675
Marketed since
May 18, 2023
Listing expires
December 31, 2027
Pharmacologic class
Semifluorinated Alkane

Active ingredients

Uses, dosage, side effects and warnings for Miebo →

Package NDC codes (3)

Package NDCDescriptionSince
24208-377-01 sample1 BOTTLE in 1 CARTON (24208-377-01) / 3 mg in 1 BOTTLEMay 18, 2023
24208-377-051 BOTTLE in 1 CARTON (24208-377-05) / 3 mg in 1 BOTTLEMay 18, 2023
24208-377-06 sample1 BOTTLE in 1 CARTON (24208-377-06) / 1.6 mg in 1 BOTTLEJul 19, 2024