Active Ingredient: TIMOLOL MALEATE
Proprietary Name: TIMOPTIC-XE
Dosage Form; Route of Administration: SOLUTION, GEL FORMING/DROPS; OPHTHALMIC
Strength: EQ 0.25% BASE
Reference Listed Drug: Yes
Reference Standard: No
TE Code: AB
Application Number: N020330
Product Number: 001
Approval Date: Nov 4, 1993
Applicant Holder Full Name: BAUSCH AND LOMB INC
Marketing Status:
Prescription
Patent and Exclusivity Information
