Active Ingredient: CYCLOPENTOLATE HYDROCHLORIDE
Proprietary Name: AKPENTOLATE
Dosage Form; Route of Administration: SOLUTION/DROPS; OPHTHALMIC
Strength: 1%
Reference Listed Drug: No
Reference Standard: No
TE Code: AT
Application Number: A040164
Product Number: 001
Approval Date: Jan 13, 1997
Applicant Holder Full Name: RISING PHARMA HOLDINGS INC
Marketing Status:
Prescription
Patent and Exclusivity Information