Active Ingredient: PREDNISOLONE SODIUM PHOSPHATE
Proprietary Name: PREDNISOLONE SODIUM PHOSPHATE
Dosage Form; Route of Administration: SOLUTION/DROPS; OPHTHALMIC
Strength: EQ 0.11% PHOSPHATE
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A084171
Product Number: 001
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: SOLA BARNES HIND
Marketing Status:
Discontinued
Patent and Exclusivity Information