Active Ingredient: CYCLOPENTOLATE HYDROCHLORIDE
Proprietary Name: CYCLOPENTOLATE HYDROCHLORIDE
Dosage Form; Route of Administration: SOLUTION/DROPS; OPHTHALMIC
Strength: 1%
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A089162
Product Number: 001
Approval Date: Jan 24, 1991
Applicant Holder Full Name: ALCON PHARMACEUTICALS LTD
Marketing Status:
Discontinued
Patent and Exclusivity Information