Active Ingredient: PREDNISOLONE ACETATE; SULFACETAMIDE SODIUM
Proprietary Name: PREDAMIDE
Dosage Form; Route of Administration: SUSPENSION/DROPS; OPHTHALMIC
Strength: 0.5%;10%
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A088059
Product Number: 001
Approval Date: Jul 29, 1983
Applicant Holder Full Name: EPIC PHARMA LLC
Marketing Status:
Discontinued
Patent and Exclusivity Information
