Active Ingredient: PREDNISOLONE SODIUM PHOSPHATE; SULFACETAMIDE SODIUM
Proprietary Name: SULFACETAMIDE SODIUM AND PREDNISOLONE SODIUM PHOSPHATE
Dosage Form; Route of Administration: SOLUTION/DROPS; OPHTHALMIC
Strength: EQ 0.23% PHOSPHATE;10%
Reference Listed Drug: No
Reference Standard: Yes
TE Code:
Application Number: A074449
Product Number: 001
Approval Date: Dec 29, 1995
Applicant Holder Full Name: BAUSCH AND LOMB INC
Marketing Status:
Prescription
Patent and Exclusivity Information