Active Ingredient: SULFACETAMIDE SODIUM
Proprietary Name: SULF-15
Dosage Form; Route of Administration: SOLUTION/DROPS; OPHTHALMIC
Strength: 15%
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A089047
Product Number: 001
Approval Date: Oct 31, 1995
Applicant Holder Full Name: NOVARTIS PHARMACEUTICALS CORP
Marketing Status:
Discontinued
Patent and Exclusivity Information