Active Ingredient: DIPIVEFRIN HYDROCHLORIDE
Proprietary Name: DIPIVEFRIN HYDROCHLORIDE
Dosage Form; Route of Administration: SOLUTION/DROPS; OPHTHALMIC
Strength: 0.1%
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A074188
Product Number: 001
Approval Date: May 19, 1995
Applicant Holder Full Name: BAUSCH AND LOMB PHARMACEUTICALS INC
Marketing Status:
Discontinued
Patent and Exclusivity Information