Active Ingredient: TRAVOPROST
Proprietary Name: TRAVATAN
Dosage Form; Route of Administration: SOLUTION/DROPS; OPHTHALMIC
Strength: 0.004% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**
Reference Listed Drug: Yes
Reference Standard: No
TE Code:
Application Number: N021257
Product Number: 001
Approval Date: Mar 16, 2001
Applicant Holder Full Name: ALCON PHARMACEUTICALS LTD
Marketing Status:
Discontinued
Patent and Exclusivity Information