Travoprost Ophthalmic

Product NDC
72162-2432
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Travoprost Ophthalmic Solution
Dosage form
SOLUTION
Route
OPHTHALMIC
Labeler
Bryant Ranch Prepack
Application
ANDA203767
Marketing category
ANDA
Substance
TRAVOPROST
Current FDA listing
Yes

Related Records

Packages

Package NDCDescriptionMarketing startMarketing endSampleStatus
72162-2432-21 BOTTLE in 1 CARTON (72162-2432-2) / 2.5 mL in 1 BOTTLE20241216NoHistorical
72162-2432-41 BOTTLE in 1 CARTON (72162-2432-4) / 5 mL in 1 BOTTLE20241216NoHistorical

Related DailyMed Labels

Set IDTitleManufacturerEffective dateTypeVersion
2d95e26f-7cdd-462f-b32f-10cb68424aaaThese highlights do not include all the information needed to use TRAVOPROST OPHTHALMIC SOLUTION (Ionic Buffered Solution) safely and effectively. See full prescribing information for TRAVOPROST OPHTHALMIC SOLUTION (Ionic Buffered Solution). TRAVOPROST ophthalmic solution (ionic buffered solution), for topical ophthalmic use Initial U.S. Approval: 2001Bryant Ranch Prepack2026-03-16HUMAN PRESCRIPTION DRUG LABEL102