Active Ingredient: TIMOLOL MALEATE
Proprietary Name: TIMOLOL MALEATE
Dosage Form; Route of Administration: SOLUTION, GEL FORMING/DROPS; OPHTHALMIC
Strength: EQ 0.25% BASE
Reference Listed Drug: No
Reference Standard: No
TE Code: AB
Application Number: A215733
Product Number: 001
Approval Date: Sep 22, 2022
Applicant Holder Full Name: DR REDDYS LABORATORIES LTD
Marketing Status:
Prescription
Patent and Exclusivity Information