Active Ingredient: PREDNISOLONE SODIUM PHOSPHATE
Proprietary Name: PREDAIR
Dosage Form; Route of Administration: SOLUTION/DROPS; OPHTHALMIC
Strength: EQ 0.11% PHOSPHATE
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A088415
Product Number: 001
Approval Date: Feb 29, 1984
Applicant Holder Full Name: PHARMAFAIR INC
Marketing Status:
Discontinued
Patent and Exclusivity Information