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:
Application Number: A088150
Product Number: 001
Approval Date: Feb 25, 1983
Applicant Holder Full Name: PHARMAFAIR INC
Marketing Status:
Discontinued
Patent and Exclusivity Information