Active Ingredient: CYCLOPENTOLATE HYDROCHLORIDE
Proprietary Name: PENTOLAIR
Dosage Form; Route of Administration: SOLUTION/DROPS; OPHTHALMIC
Strength: 1%
Reference Listed Drug: No
Reference Standard: No
TE Code: AT
Application Number: A040075
Product Number: 001
Approval Date: Apr 29, 1994
Applicant Holder Full Name: BAUSCH AND LOMB PHARMACEUTICALS INC
Marketing Status:
Prescription
Patent and Exclusivity Information