Active Ingredient: CYCLOPENTOLATE HYDROCHLORIDE
Proprietary Name: AK-PENTOLATE
Dosage Form; Route of Administration: SOLUTION/DROPS; OPHTHALMIC
Strength: 1%
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A085555
Product Number: 001
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: EPIC PHARMA LLC
Marketing Status:
Discontinued
Patent and Exclusivity Information