Active Ingredient: HYDROCORTISONE; NEOMYCIN SULFATE; POLYMYXIN B SULFATE
Proprietary Name: NEOMYCIN AND POLYMYXIN B SULFATES AND HYDROCORTISONE
Dosage Form; Route of Administration: SUSPENSION/DROPS; OPHTHALMIC
Strength: 1%;EQ 3.5MG BASE/ML;10,000 UNITS/ML
Reference Listed Drug: No
Reference Standard: Yes
TE Code:
Application Number: A062874
Product Number: 001
Approval Date: May 11, 1988
Applicant Holder Full Name: SANDOZ INC
Marketing Status:
Prescription
Patent and Exclusivity Information