Active Ingredient: CYCLOPENTOLATE HYDROCHLORIDE
Proprietary Name: PENTOLAIR
Dosage Form; Route of Administration: SOLUTION/DROPS; OPHTHALMIC
Strength: 0.5%
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A088643
Product Number: 001
Approval Date: Feb 9, 1987
Applicant Holder Full Name: PHARMAFAIR INC
Marketing Status:
Discontinued
Patent and Exclusivity Information