Active Ingredient: DEXAMETHASONE; NEOMYCIN SULFATE; POLYMYXIN B SULFATE
Proprietary Name: MAXITROL
Dosage Form; Route of Administration: SUSPENSION/DROPS; OPHTHALMIC
Strength: 0.1%;EQ 3.5MG BASE/ML;10,000 UNITS/ML
Reference Listed Drug: No
Reference Standard: No
TE Code: AT
Application Number: A062341
Product Number: 001
Approval Date: May 22, 1984
Applicant Holder Full Name: SANDOZ INC
Marketing Status:
Prescription
Patent and Exclusivity Information
