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: No
TE Code:
Application Number: A079186
Product Number: 001
Approval Date: Nov 18, 2009
Applicant Holder Full Name: AMERICAN REGENT INC
Marketing Status:
Discontinued
Patent and Exclusivity Information
