Active Ingredient: SULFACETAMIDE SODIUM
Proprietary Name: SULF-10
Dosage Form; Route of Administration: SOLUTION/DROPS; OPHTHALMIC
Strength: 10%
Reference Listed Drug: No
Reference Standard: No
TE Code:
Application Number: A080025
Product Number: 001
Approval Date: Approved Prior to Jan 1, 1982
Applicant Holder Full Name: NOVARTIS PHARMACEUTICALS CORP
Marketing Status:
Discontinued
Patent and Exclusivity Information
