Active Ingredient: DORZOLAMIDE HYDROCHLORIDE
Proprietary Name: DORZOLAMIDE HYDROCHLORIDE
Dosage Form; Route of Administration: SOLUTION/DROPS; OPHTHALMIC
Strength: EQ 2% BASE
Reference Listed Drug: No
Reference Standard: Yes
TE Code: AT
Application Number: A204778
Product Number: 001
Approval Date: Nov 8, 2019
Applicant Holder Full Name: MICRO LABS LTD
Marketing Status:
Prescription
Patent and Exclusivity Information
