Active Ingredient: PREDNISOLONE ACETATE; SULFACETAMIDE SODIUM
Proprietary Name: PREDSULFAIR II
Dosage Form; Route of Administration: SUSPENSION/DROPS; OPHTHALMIC
Strength: 0.2%;10%
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A088837
Product Number: 001
Approval Date: Dec 24, 1985
Applicant Holder Full Name: PHARMAFAIR INC
Marketing Status:
Discontinued
Patent and Exclusivity Information
